Xonvea

Xonvea contains two active substances: doxylamine succinate, which belongs to a group of medicines called antihistamines, and pyridoxine hydrochloride, another name for vitamin B6. Xonvea is used for Nausea and vomiting of pregnancy (NVP).

Also called: Diclegis (United States) · Diclectin (Canada)

Pronunciation: pronunciation varies by local usage.

Generic name
doxylamine succinate / pyridoxine hydrochloride
Brand names
Xonvea
Drug class
Antihistamine (doxylamine succinate, an ethanolamine-derivative antihistamine) combined with pyridoxine hydrochloride (vitamin B6)
Form
Gastro-resistant tablets, each containing 10 mg doxylamine succinate and 10 mg pyridoxine hydrochloride; white, round, film-coated tablets with a pink image of a pregnant woman on one side; blister packs of 20, 30 or 40 tablets (not all pack sizes may be marketed)
Route
Oral
Legal status
Prescription-only medicine (UK)

Availability and supply rules vary by country

Trade names by country: United States · United Kingdom · Canada · Australia

Australia: Debendox (historical, withdrawn 1983); individual ingredients available OTC separately · Full directory

What doxylamine succinate / pyridoxine hydrochloride is and how it works

Xonvea contains two active substances: doxylamine succinate, which belongs to a group of medicines called antihistamines, and pyridoxine hydrochloride, another name for vitamin B6. It is used in pregnant women aged 18 years and older to help stop them feeling sick (nausea) and being sick (vomiting), when changes in diet or other non-medicine treatments have not worked. (1) (2)

Xonvea is indicated for the treatment of nausea and vomiting of pregnancy (NVP) in pregnant women aged 18 years or older who do not respond to conservative management (lifestyle and diet change). It should be taken as a daily prescription and not on an as-needed basis. Continued need should be reassessed as the pregnancy progresses. Xonvea is not indicated for use in children under 18 years of age.

Mechanism of action: how doxylamine succinate / pyridoxine hydrochloride works

Xonvea contains two active substances: doxylamine succinate, an antihistamine (ethanolamine-derivative), and pyridoxine hydrochloride, also known as vitamin B6. Doxylamine succinate has anticholinergic properties. Full pharmacological properties (section 5) were not quoted in the supplied research notes beyond the statement that section 5 of the SmPC is the pharmacological properties section; no further pharmacology detail can be stated. (1) (2)

What is Doxylamine succinate / pyridoxine hydrochloride used for?

Nausea and vomiting of pregnancy (NVP)

Xonvea is indicated for the treatment of nausea and vomiting of pregnancy (NVP) in pregnant women >=18 years who do not respond to conservative management (i.e. lifestyle and diet change). (1) (2)

Before taking doxylamine succinate / pyridoxine hydrochloride

Do not take / not appropriate for

  • Do not take Xonvea if you are allergic (hypersensitive) to doxylamine succinate, other ethanolamine-derivative antihistamines (such as diphenhydramine), pyridoxine hydrochloride or any of the other ingredients of this medicine. (all patients) (1) (2)
  • Do not take Xonvea if you are taking medicines for depression called monoamine oxidase inhibitors (MAOIs). Concomitant use with MAOIs is contraindicated. (all patients) (1) (2)

Tell your clinician about

  • If you have ever had: asthma; increased eye pressure; an eye problem called narrow angle glaucoma; a stomach ulcer (stenosing peptic ulcer); a blockage in your gut between your stomach and small intestine (pyloroduodenal obstruction); or a blockage in your bladder (bladder-neck obstruction) - Xonvea has anticholinergic properties and should be used with caution in these patients.
  • If you are taking cough or cold medicines, sleeping medicines or certain pain medicines (central nervous system depressants), because using any of these with Xonvea can make you feel very sleepy and this can make you fall over or cause other accidents.
  • If you have been drinking alcohol. Use of Xonvea is not recommended if a woman is concurrently using central nervous system (CNS) depressants including alcohol.
  • If you are taking any additional vitamin B, through your diet, from supplements or multivitamins - Xonvea contains pyridoxine hydrochloride, a vitamin B6 analogue, so additional levels from diet and vitamin B6 supplements should be assessed.
  • If you are having a urine drug screen - Xonvea may show false positive results for methadone, opiates, and phencyclidine phosphate (PCP) when some test methods are used; a more specific confirmatory test can be performed.
  • If you suffer from severe nausea and vomiting of pregnancy, a condition called hyperemesis gravidarum, you have to be treated by a specialist, because there is limited evidence in cases of hyperemesis gravidarum for the combination doxylamine/pyridoxine.
  • If you cannot swallow Xonvea tablets whole, tell your doctor, pharmacist or nurse.
  • If you are breastfeeding, or plan to breastfeed - a decision should be made with your doctor.
  • This medicine contains the azo colouring agent Allura red AC aluminium lake (E 129), which may cause allergic reactions.
(1) (2)

Doxylamine succinate / pyridoxine hydrochloride dosage and how to take it

  • Always take this medicine exactly as your doctor, pharmacist or nurse has told you. Check with your doctor, pharmacist or nurse if you are not sure.
  • Your doctor will start you on a low dose and possibly increase it - this will depend on how well the medicine works for you.
  • Day 1: take 2 tablets by mouth at bedtime (recommended starting dose: total dose 20 mg doxylamine succinate / 20 mg pyridoxine hydrochloride).
  • Day 2: take 2 tablets by mouth at bedtime. If your nausea and vomiting is better or controlled on Day 2, continue to take 2 tablets every night at bedtime; this will be your usual dose unless your doctor, pharmacist or nurse tells you otherwise.
  • Day 3: if you still had nausea and vomiting on Day 2, take 1 tablet in the morning and 2 tablets at bedtime, by mouth.
  • Day 4: if your nausea and vomiting was better or controlled on Day 3, continue to take 1 tablet in the morning and 2 tablets at bedtime by mouth each day; this will be your usual dose unless your doctor, pharmacist or nurse tells you otherwise.
  • Day 4: if you still had nausea and vomiting on Day 3, take 1 tablet in the morning, 1 tablet in the mid-afternoon, and 2 tablets at bedtime, by mouth. This will be your usual dose unless your doctor, pharmacist or nurse tells you otherwise.
  • The maximum recommended daily dose is 4 tablets (1 in the morning, 1 in the mid-afternoon and 2 at bedtime). Do not take more than 4 tablets each day.
  • Xonvea should be taken on an empty stomach with a glass of water. A food-effect study has shown that the delay in onset of action may be further delayed, and a reduction in absorption may occur, when tablets are taken with food.
  • Swallow the tablet whole with a glass of water. Do not crush, chew or split the tablets before swallowing, to preserve the effect of this medicine and the gastro-resistant properties.
  • Xonvea should be taken as a daily prescription and not on an as needed basis.
  • Continued need for Xonvea should be reassessed as the pregnancy progresses.
  • Do not change the dose yourself; follow the schedule your doctor, pharmacist or nurse has told you.
(1) (2)

Procedures and treatment changes

Tell the treating team before surgery, procedures, or any medicine change. Do not alter treatment without the responsible clinician. (1) (2) (3)

Missed dose

Follow the exact product instructions and do not double a dose.

Overdose

Xonvea is a delayed-release formulation; therefore, signs and symptoms may not be apparent immediately. If you take more Xonvea than you should, seek medical attention promptly - talk to a doctor or go to a hospital straight away, even if you feel well, and take the medicine pack with you. Signs and symptoms of overdosage may include restlessness, dryness of mouth, dilated pupils, sleepiness, vertigo, mental confusion and tachycardia. At toxic doses, doxylamine exhibits anticholinergic effects, including seizures, rhabdomyolysis, acute renal failure and death. In the event of an overdose, management consists of activated charcoal, whole bowel irrigation and symptomatic treatment, in accordance with established treatment guidelines. Fatalities have been reported from doxylamine overdose in children; children appear to be at high risk for cardiorespiratory arrest and a toxic dose for children of more than 1.8 mg/kg has been reported. Let the clinician you see advise on whether to continue or stop, and on any further treatment. (1) (2)

Doxylamine succinate / pyridoxine hydrochloride side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them. Adverse event information is derived from clinical trials and worldwide post-marketing experience; the incidence of treatment-emergent adverse events was similar for both treatment and placebo groups. The most frequently reported adverse reaction (>=5% and exceeding the rate in placebo) was somnolence. Frequency of adverse reactions reported during post-marketing use cannot be determined as they are derived from spontaneous reports and are therefore qualified as 'not known'.

Somnolence (feeling very sleepy)

What to notice: Feeling very sleepy. Somnolence is very common (may affect more than 1 in 10 people) and is due to the anticholinergic properties of doxylamine succinate.

What to do: Do not drive, cycle or use any tools or machines while taking this medicine. Tell your doctor, pharmacist or nurse if this is troublesome. (1) (2)

Dizziness

What to notice: Feeling dizzy (common: may affect up to 1 in 10 people).

What to do: Avoid activities requiring complete mental alertness until cleared to do so by your healthcare provider. Tell your doctor, pharmacist or nurse if it is persistent or troublesome. (1) (2)

Fatigue

What to notice: Feeling tired (common: may affect up to 1 in 10 people).

What to do: Tell your doctor, pharmacist or nurse if it is persistent or troublesome. (1) (2)

Dry mouth

What to notice: Dry mouth (common: may affect up to 1 in 10 people).

What to do: Tell your doctor, pharmacist or nurse if it is persistent or troublesome. (1) (2)

Hypersensitivity (allergic reaction) to Xonvea

What to notice: Hypersensitivity (allergic reaction). Frequency not known.

What to do: Contact your doctor, pharmacist or nurse promptly for assessment. (1) (2)

Severe drowsiness from taking Xonvea with CNS depressants or alcohol

What to notice: Severe drowsiness may occur if Xonvea is taken along with CNS depressants including alcohol, hypnotic sedatives and tranquilizers.

What to do: Contact your doctor or pharmacist promptly; avoid alcohol and CNS depressants, as concurrent use is not recommended. (1) (2)

Other adverse reactions with frequency 'not known'

What to notice: Psychiatric: anxiety, disorientation, insomnia, nightmares. Nervous system: headache, migraines, paresthesia, psychomotor hyperactivity. Eye: blurred vision, visual disturbances. Ear and labyrinth: vertigo. Cardiac: dyspnea, palpitation, tachycardia. Gastrointestinal: abdominal distention, abdominal pain, constipation, diarrhoea. Skin: hyperhidrosis, pruritus, rash, rash maculo-papular. Renal and urinary: dysuria, urinary retention. General: chest discomfort, irritability, malaise.

What to do: Talk to your doctor, pharmacist or nurse about these, including any possible side effects not listed. (1) (2)

Anticholinergic class effects

What to notice: Possible adverse anticholinergic effects associated with the use of antihistamines as a class include: dryness of mouth, nose and throat; dysuria; urinary retention; vertigo; visual disturbances; blurred vision; diplopia; tinnitus; acute labyrinthitis; insomnia; tremors; nervousness; irritability; and facial dyskinesia. Tightness of chest, thickening of bronchial secretions, wheezing, nasal stuffiness, sweating, chills, early menses, toxic psychosis, headache, faintness and paresthesia have occurred.

What to do: Talk to your doctor, pharmacist or nurse if you experience these effects. (1) (2)

Serious warnings

Driving and operating machines — major

Symptoms: Xonvea has a moderate to major influence on the ability to drive and use machines. You may feel sleepy after taking Xonvea.

Action: Do not drive, cycle or use any tools or machines while taking this medicine. Avoid engaging in activities requiring complete mental alertness until cleared to do so by your healthcare provider. If this happens do not do other activities that need your full attention unless your doctor tells you it is ok to do so. (1) (2)

Severe drowsiness with CNS depressants or alcohol — serious

Symptoms: Severe drowsiness may occur if Xonvea is taken along with CNS depressants including alcohol, hypnotic sedatives and tranquilizers. This can make you fall over or cause other accidents.

Action: Concurrent use with CNS depressants including alcohol is not recommended. Do not drink alcohol while taking Xonvea. Talk to your doctor or pharmacist before taking cough or cold medicines, sleeping medicines or certain pain medicines. (1) (2)

MAOI interaction — contraindicated

Symptoms: MAOIs prolong and intensify the anticholinergic effects of antihistamines.

Action: Concomitant treatment with MAOIs is contraindicated. Do not take Xonvea if you are taking an MAOI; tell your doctor, pharmacist or nurse. (1) (2)

Overdose of a delayed-release formulation — emergency

Symptoms: Restlessness, dryness of mouth, dilated pupils, sleepiness, vertigo, mental confusion and tachycardia. At toxic doses, doxylamine exhibits anticholinergic effects including seizures, rhabdomyolysis, acute renal failure and death. In children, fatalities have been reported, characterised by coma, grand mal seizures and cardiorespiratory arrest.

Action: Seek emergency care promptly if an overdose is suspected, even if you feel well, and take the medicine pack. Symptoms may not be apparent immediately because Xonvea is a delayed-release formulation. Management consists of activated charcoal, whole bowel irrigation and symptomatic treatment, in accordance with established treatment guidelines. (1) (2)

Breastfeeding — special_population

Symptoms: The molecular weight of doxylamine succinate is low enough that passage into breast milk can be expected. Excitement, irritability and sedation have been reported in nursing infants presumably exposed to doxylamine succinate through breast milk. Infants with apnoea or other respiratory syndromes may be particularly vulnerable to the sedative effects of Xonvea, resulting in worsening of their apnoea or respiratory conditions. Pyridoxine hydrochloride is excreted into breast milk; there have been no reports of adverse events in infants presumably exposed to pyridoxine hydrochloride through breast milk. A risk to breastfed infants cannot be excluded.

Action: A decision must be made whether to discontinue breast-feeding or to discontinue/abstain from Xonvea therapy, taking into account the benefit of breast feeding for the child and the benefit of therapy for the woman, with your doctor. Let the clinician you see advise on whether to continue or stop. (1) (2)

Interactions

Medicine or testEffectAction
Monoamine oxidase inhibitors (MAOIs)MAOIs prolong and intensify the anticholinergic effects of antihistamines. Concomitant treatment is contraindicated.Do not take Xonvea if you are taking an MAOI. Tell your doctor or pharmacist or nurse if you are taking any of these medicines. (1) (2)
Central nervous system (CNS) depressants including alcohol, hypnotic sedatives and tranquilizersConcurrent use is not recommended; the combination may result in severe drowsiness. This can make you fall over or cause other accidents.Do not drink alcohol while taking Xonvea. Tell your doctor, pharmacist or nurse if you are taking cough or cold medicines, sleeping medicines or certain pain medicines. (1) (2)
FoodA food-effect study has demonstrated that the delay in the onset of action of Xonvea may be further delayed, and a reduction in absorption may occur, when tablets are taken with food.Xonvea should be taken on an empty stomach with a glass of water. (1) (2)
Interference with urine screen for methadone, opiates and PCPFalse positive urine drug screens for methadone, opiates, and phencyclidine phosphate (PCP) can occur with doxylamine succinate/pyridoxine hydrochloride use.Confirmatory tests, such as Gas Chromatography Mass Spectrometry (GC-MS), should be used to confirm the identity of the substance in the event of a positive immunoassay result. (1) (2)

Pregnancy, breastfeeding, kidney/liver function, age

Children and adolescents

Xonvea is not indicated for use in children under 18 years of age. The safety and efficacy of Xonvea has not been established in that population. No data are available. (1) (2)

Pregnancy

Xonvea is intended for use in pregnant women. A large amount of data on pregnant women, including two meta-analyses with over 168,000 patients and 18,000 exposures to the doxylamine/pyridoxine combination during the first trimester, indicates no malformative nor feto/neonatal toxicity of doxylamine succinate and pyridoxine hydrochloride. (1) (2)

Breastfeeding

The molecular weight of doxylamine succinate is low enough that passage into breast milk can be expected. Excitement, irritability and sedation have been reported in nursing infants presumably exposed to doxylamine succinate through breast milk. Infants with apnoea or other respiratory syndromes may be particularly vulnerable to the sedative effects of Xonvea, resulting in worsening of their apnoea or respiratory conditions. Pyridoxine hydrochloride is excreted into breast milk; there have been no reports of adverse events in infants presumably exposed to pyridoxine hydrochloride through breast milk. A risk to breastfed infants cannot be excluded. A decision must be made whether to discontinue breast-feeding or to discontinue/abstain from Xonvea therapy, taking into account the benefit of breast feeding for the child and the benefit of therapy for the woman. Discuss with your doctor. (1) (2)

Fertility

Xonvea caused no impairment of fertility or reproductive performance in rats. No human data are available. (1)

Hyperemesis gravidarum

There is limited evidence in cases of hyperemesis gravidarum for the combination doxylamine/pyridoxine. These patients should be treated by a specialist. (1) (2)

Patients with conditions where anticholinergic caution applies

Xonvea has anticholinergic properties and should be used with caution in patients with: asthma, increased intraocular pressure, narrow angle glaucoma, stenosing peptic ulcer, pyloroduodenal obstruction and bladder-neck obstruction. (1) (2)

Monitoring

Before starting

  • Confirm the patient is a pregnant woman aged 18 years or older with nausea and vomiting of pregnancy who has not responded to conservative management (lifestyle and diet change).
  • Assess for hypersensitivity to doxylamine succinate, other ethanolamine-derivative antihistamines, pyridoxine hydrochloride or any excipients.
  • Check for concomitant use of MAOIs (contraindicated) and of CNS depressants including alcohol, hypnotic sedatives and tranquilizers (not recommended).
  • Assess additional vitamin B6 intake from diet and vitamin B6 supplements.
  • Assess the conditions requiring caution due to anticholinergic properties: asthma, increased intraocular pressure, narrow angle glaucoma, stenosing peptic ulcer, pyloroduodenal obstruction and bladder-neck obstruction.
  • Confirm the patient can swallow the gastro-resistant tablets whole.
  • Consider specialist referral if hyperemesis gravidarum is suspected, because evidence is limited in this population.

During treatment

  • Reassess continued need for Xonvea as the pregnancy progresses.
  • Reassess symptom control to determine whether the dose should be increased as per the day 1 to day 4 schedule, or whether the usual dose continues.
  • Advise avoidance of driving, cycling and use of tools or machines while taking Xonvea until cleared by the healthcare provider.
  • Reassess concurrent use of CNS depressants, alcohol and additional vitamin B6 intake.
  • At the time of discontinuation, use a gradual tapering dose to prevent a sudden return of nausea and vomiting of pregnancy symptoms; the doctor will tell the patient how to stop the medicine slowly over time.
(1) (2)

Storage

This medicine does not require any special storage conditions. Keep this medicine out of the sight and reach of children. Do not use this medicine after the expiry date which is stated on the carton or blister after 'EXP'. The expiry date refers to the last day of that month. Do not throw away any medicines via wastewater or household waste; ask your pharmacist how to throw away medicines you no longer use.

Professional information

Clinician-facing context only. Use the current UK Summary of Product Characteristics and local prescribing information. This page does not provide personalised medical advice.

UK

Indication: Nausea and vomiting of pregnancy (NVP) in pregnant women >=18 years who do not respond to conservative management

Dose summary: Recommended starting dose is two tablets (total dose: 20 mg doxylamine succinate / 20 mg pyridoxine hydrochloride) at bedtime (Day 1). If this dose adequately controls symptoms the next day, continue two tablets at bedtime. If symptoms persist into the afternoon of Day 2, continue two tablets at bedtime on Day 2 and on Day 3 take three tablets (one tablet in the morning and two tablets at bedtime). If three tablets do not adequately control symptoms on Day 3, take four tablets starting on Day 4 (one tablet in the morning, one tablet mid-afternoon and two tablets at bedtime). Maximum recommended daily dose is four tablets (one in the morning, one in the mid-afternoon and two at bedtime). Take on an empty stomach with a glass of water; swallow whole without crushing, splitting or chewing.

Renal context: Not addressed in the supplied research notes; no renal dosing information can be stated. This is an unresolved gap. (1) (2)

Mechanism of action

Hepatic guidance

Not addressed in the supplied research notes; no hepatic dosing information can be stated. This is an unresolved gap.

Overdose note

Xonvea is a delayed-release formulation, so signs and symptoms may not be apparent immediately. Symptoms may include restlessness, dryness of mouth, dilated pupils, sleepiness, vertigo, mental confusion and tachycardia; at toxic doses, anticholinergic effects including seizures, rhabdomyolysis, acute renal failure and death. Management consists of activated charcoal, whole bowel irrigation and symptomatic treatment in accordance with established treatment guidelines. (1) (2)

Frequently asked questions

What is Xonvea used for?

Xonvea is used in pregnant women aged 18 years and older to help stop them feeling sick (nausea) and being sick (vomiting), when changes in diet or other non-medicine treatments have not worked. (1) (2)

Can I stop taking Xonvea suddenly?

Do not stop taking Xonvea without talking to your doctor first. If you stop taking this medicine suddenly your feeling sick (nausea) and being sick (vomiting) may come back. Your doctor will tell you how to stop taking this medicine slowly over time to help avoid this. To prevent a sudden return of symptoms, a gradual tapering dose is recommended at the time of discontinuation. (1) (2)

Can I drive while taking Xonvea?

No. Do not drive, cycle or use any tools or machines while taking this medicine, because you may feel sleepy. Xonvea has a moderate to major influence on the ability to drive and use machines. Avoid activities requiring complete mental alertness until cleared to do so by your healthcare provider. (1) (2)

Should Xonvea be taken with or without food?

Take Xonvea on an empty stomach with a glass of water. A food-effect study showed that the delay in onset of action may be further delayed, and a reduction in absorption may occur, when tablets are taken with food. Swallow the tablet whole; do not crush, chew or split the tablets before swallowing. (1) (2)

Can Xonvea affect a urine drug screen?

Yes. Taking Xonvea may show 'false positive' results for methadone, opiates, and phencyclidine phosphate (PCP) when some test methods are used. If this happens, a more specific test can be performed (for example Gas Chromatography Mass Spectrometry, GC-MS). (1) (2)

Can I take Xonvea with other medicines for cough, cold, sleep or pain?

Talk to your doctor or pharmacist or nurse before taking Xonvea if you are taking cough or cold medicines, sleeping medicines or certain pain medicines, because using any of these with Xonvea can make you feel very sleepy and this can make you fall over or cause other accidents. Also, do not take Xonvea with medicines for depression called monoamine oxidase inhibitors (MAOIs), as this combination is contraindicated. (1) (2)

What is the maximum daily dose of Xonvea?

The maximum recommended daily dose is 4 tablets (1 in the morning, 1 in the mid-afternoon, and 2 at bedtime). Do not take more than 4 tablets each day. (1) (2)

What is the mechanism of action of doxylamine succinate / pyridoxine hydrochloride?

Xonvea contains two active substances: doxylamine succinate, an antihistamine (ethanolamine-derivative), and pyridoxine hydrochloride, also known as vitamin B6. Doxylamine succinate has anticholinergic properties. Full pharmacological properties (section 5) were not quoted in the supplied research notes beyond the statement that section 5 of the SmPC is the pharmacological properties section; no further pharmacology detail can be stated. (1) (2)

What is the generic name of Xonvea?

The generic name is doxylamine succinate / pyridoxine hydrochloride. It is sold under brand names including Xonvea. (1) (2) (3)

What class of drug is doxylamine succinate / pyridoxine hydrochloride?

Xonvea is classed as: Antihistamine (doxylamine succinate, an ethanolamine-derivative antihistamine) combined with pyridoxine hydrochloride (vitamin B6). (1) (2) (3)

References

  1. Xonvea 10 mg/10 mg gastro-resistant tablets — Summary of Product Characteristicselectronic Medicines Compendium (UK), Exeltis UK · United Kingdom · accessed 2026-10-13 · source 1
  2. Xonvea 10 mg/10 mg gastro-resistant tablets — Package leaflet: Information for the userelectronic Medicines Compendium (UK), Exeltis UK · United Kingdom · accessed 2026-10-13 · source 2
  3. DICLEGIS (doxylamine succinate and pyridoxine hydrochloride) delayed-release tablets — prescribing informationDailyMed, U.S. National Library of Medicine · United States · accessed 2026-10-13 · source 3

Brand names by country

Single-ingredient doxylamine succinate / pyridoxine hydrochloride names are shown separately by country. Product availability, strengths, and supply rules can change; combination products are not included here.

Priority countries

United States

  • DiclegisFDA approved prescription label confirmed · 10 mg/10 mg · Duchesnay USA

United Kingdom

  • XonveaMHRA marketing authorisation PL 16853 0147 confirmed · 10 mg/10 mg · Alliance Pharmaceuticals Limited

Canada

  • Diclectincurrent health canada product monograph confirmed · 10 mg/10 mg · not specified in fetched source

Australia

  • Debendox (historical, withdrawn 1983); individual ingredients available OTC separatelyreal historical withdrawal no current combination product artg entry found · not specified · not specified
View brands in additional countries.

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