Cetirizine Hydrochloride by Chain Drug Consortium, LLC
Medically reviewed on September 6, 2017
Dosage form: tablet, chewable
Ingredients: CETIRIZINE HYDROCHLORIDE 10mg
Labeler: Chain Drug Consortium, LLC
NDC Code: 68016-353
Cetirizine hydrochloride, USP 10 mg
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- runny nose
- itchy, watery eyes
- itching of the nose or throat
if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.
liver or kidney disease. Your doctor should determine if you need a different dose.
you are taking tranquilizers or sedatives.
- drowsiness may occur
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase drowsiness
- be careful when driving a motor vehicle or operating machinery
an allergic reaction to this product occurs. Seek medical help right away.
- if breast-feeding: not recommended
- if pregnant: ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
- may be taken with or without water
|adults and children 6 years and over||one 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 over||ask a doctor
|children under 6 years of age||ask a doctor
|consumers with liver or kidney disease||ask a doctor
- store between 20° to 25°C (68° to 77°F)
- do not use if inner safety seal is open or torn
- see top layer for lot number and expiration date
acesulfame potassium, colloidal silicon dioxide, compressible sugar, crospovidone, FD & C Blue No # 2 Aluminum Lake, FD & C Red No # 40 Aluminum Lake, guar gum, magnesium oxide light powder, magnesium stearate, mannitol, microcrystalline cellulose, pregelatinized starch, prosweet N & A flavor powder, talc, tutti frutti flavor
Call toll free 1-800-818-4555 weekdays
cetirizine hydrochloride tablet, chewable
|Labeler - Chain Drug Consortium, LLC (101668460)|
|Registrant - Sun Pharmaceutical Industries Limited (650172430)|
|Sun Pharmaceutical Industries Limited||725959238||MANUFACTURE(68016-353)|
Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.