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Drug Facts


OTC - ACTIVE INGREDIENT SECTION

Cetirizine HCl 5 mg

Cetirizine HCl 10 mg


OTC - PURPOSE SECTION

Antihistamine


INDICATIONS & USAGE SECTION

Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • •runny nose, 
  • •sneezing,
  • •itchy, watery eyes,
  • •itching of the nose or throat

WARNINGS SECTION

Do not use if you have ever had an allergic reaction to this product or any of its ingredients or an antihistamine containing hydroxyzine

Ask a doctor before useif you have liver or kidney disease. 

Your doctor should determine if you need a different dose.

Ask a doctor or pharmacist before use if you are taking tranquilizers or sedatives

When using this product

Stop use and ask a doctor if an allergic reaction to this product occurs.  Seek medical help right away.

If pregnant or breast-feeding:

  • •drowsiness may occur
  • •avoid alcoholic drinks
  • •alcohol, sedatives, and tranquilizers may increase drowsiness
  • •be careful when driving a motor vehicle or operating machinery

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222)


DOSAGE & ADMINISTRATION SECTION

Cetirizine Hydrochloride Tablets, USP 5 mg

Cetirizine Hydrochloride Tablets, USP 10 mg

adults and children 6 years and over1 tablet (5 mg) or 2 tablets (10) once daily depending upon severity of symptoms; do not take more than 2 tablets (10) in 24 hours.
adults 65 years and over1 tablet (5 mg) once a day; do not take more than 1 tablet (5 mg) in 24 hours.
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor
adults and children 6 years and overone 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours.A 5 mg product may be appropriate for less severe symptoms.
adults 65 years and overask a doctor
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Other information

  • •store between 20°C to 25°C (68°F to 77°F)
  • •do not use of imprinted foil inner seal on bottle is broken or missing.
  • •FDA approved organic impurities test procedure differs from USP

INACTIVE INGREDIENT SECTION

colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide


OTHER SAFETY INFORMATION

Questions or comments?

call toll-free weekdays 9 AM to 5 PM EST at 1 (888) 721-7115

Manufactured by:

Glenmark Pharmaceuticals Limited

Pithampur, Madhya Pradesh 454775, India

Distributed by:

Glenmark Therapeutics Inc., USA

Mahwah, NJ 07430

Product of India

February 2024