NDC 51660-0939-01

Cetirizine Hydrochloride 10 mg/1 TABLET

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NDC

51660-0939-01

Generic Name

Cetirizine Hydrochloride

Brand Name

Cetirizine Hydrochloride

Strength

10 mg/1

Dosage Form

TABLET

Route

ORAL

Package Size

—

Labeler

Ohm Laboratories Inc.

FDA Drug Information

Indications & Usage

Uses 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

Important Warnings

Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine. Ask a doctor before use if 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 drowsiness may occur…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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Other Cetirizine Hydrochloride NDC Codes

16571-0402-1010 mg/1TABLET

2-Day

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