Label: ALL DAY ALLERGY- cetirizine hcl capsule
- NDC Code(s): 30142-211-25, 30142-211-40, 30142-211-50
- Packager: The Kroger Co.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated November 28, 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
-
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.
When using this product
- drowsiness may occur
- alcohol, sedatives, and tranquilizers may increase drowsiness
- avoid alcoholic drinks
- be careful when driving a motor vehicle or operating machinery
Stop use and ask a doctor if
an allergic reaction to this product occurs. Seek medical help right away.
-
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 the active ingredient of ZYRTEC® *See back panel
All Day Allergy
Cetirizine HCl Capsules, 10 mg
Antihistamine
24 Hour Relief of:
- Sneezing
- Itchy, Watery Eyes
- Itchy Throat or Nose
- Runny Nose
Indoor & Outdoor Allergies
24 HOUR Symptom Relief
SOFTGELS**
(**liquid-filled capsules)
*Zyrtec® is a registered trademark of McNeil Consumer Healthcare, Fort Washington, PA 19034. McNeil Consumer Healthcare is not affiliated with The Kroger Co. or this product.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
KEEP OUTER CARD FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202
- Package Label
-
INGREDIENTS AND APPEARANCE
ALL DAY ALLERGY
cetirizine hcl capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-211 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 FD&C YELLOW NO. 6 (UNII: H77VEI93A8) GELATIN (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) MANNITOL (UNII: 3OWL53L36A) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITAN (UNII: 6O92ICV9RU) SORBITOL (UNII: 506T60A25R) Product Characteristics Color yellow Score no score Shape OVAL Size 13mm Flavor Imprint Code CET Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-211-40 1 in 1 PACKAGE 12/30/2013 02/28/2025 1 40 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:30142-211-25 1 in 1 PACKAGE 12/30/2013 02/28/2025 2 25 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:30142-211-50 1 in 1 PACKAGE 12/30/2013 02/28/2025 3 50 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 NDA NDA022429 12/30/2013 02/28/2025 Labeler - The Kroger Co. (006999528)
