Label: ALLERGY RELIEF- cetirizine hcl capsule, liquid filled
- NDC Code(s): 79903-344-25, 79903-344-50
- Packager: WALMART INC. (see also Equate)
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated April 29, 2025
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*
Allergy Relief
Cetirizine HCl Capsules, 10 mg
Antihistamine
Indoor & Outdoor Allergies
24-hour relief of
- Sneezing
- Runny nose
- Itchy, watery eyes
- Itchy throat or nose
SOFTGELS**
**Liquid filled capsules
*This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., 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:
Walmart Inc.,
Bentonville, AR 72716
- Product Label
-
INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
cetirizine hcl capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-344 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) ISOPROPYL ALCOHOL (UNII: ND2M416302) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITAN (UNII: 6O92ICV9RU) SORBITOL (UNII: 506T60A25R) SHELLAC (UNII: 46N107B71O) SODIUM LAURYLSULFONATE (UNII: 4GY1KJW8SI) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Product Characteristics Color yellow (Clear) Score no score Shape OVAL Size 13mm Flavor Imprint Code 291 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-344-50 1 in 1 BOX 03/31/2025 03/31/2025 1 25 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:79903-344-25 1 in 1 BOX 03/31/2025 2 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 ANDA205291 03/31/2025 Labeler - WALMART INC. (see also Equate) (051957769)

