Label: ALLERGY RELIEF- cetirizine hcl capsule
- NDC Code(s): 21130-741-25
- Packager: Safeway, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 9, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient (in each capsule)
- Purpose
- Uses
- Warning
- Do not use
- Ask a doctor before use if you have
- Ask a doctor or pharmacist before use if you are
- When using this product
- Stop use and ask a doctor if
- If pregnant or breast-feeding
- Keep out of reach of children
-
Directions
Adults and children 6 years and over One 10 mg capsule once daily; do not take more than one 10 mg capsule 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 - Other Information
- Inactive Ingredients
- Questions or comments?
-
Principal Display Panel
COMPARE TO Zyrtec® active ingredient*
24-Hour Original Prescription Strength
All Day Allergy
CETIRIZINE HCI Capsules 10 mg
Antihistamine
- Indoor & outdoor allergies
- Relief of: Sneezing, runny nose, itchy, watery eyes, itchy throat or nose
SOFTGELS**
(**liquid-filled capsules)
*This product is not manufactured or distributed by McNeil Consumer Healthcare, distributor of Zyrtec®
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
DISTRIBUTED BY:
BETTER LIVING BRANDS LLC
P.O. BOX 99, PLEASANTON, CA 94566
- Product Label
-
INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
cetirizine hcl capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-741 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength GELATIN (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) MANNITOL (UNII: 3OWL53L36A) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITAN (UNII: 6O92ICV9RU) SORBITOL (UNII: 506T60A25R) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) Product Characteristics Color yellow Score no score Shape OVAL Size 13mm Flavor Imprint Code 10 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21130-741-25 1 in 1 BOX 12/05/2018 02/28/2025 1 25 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA207235 12/05/2018 02/28/2025 Labeler - Safeway, Inc. (009137209)