Label: ALL DAY ALLERGY RELIEF- loratadine tablet
- NDC Code(s): 21130-914-10, 21130-914-12, 21130-914-60
- Packager: Safeway, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 14, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
-
Warnings
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
do not take more than directed. Taking more than directed may cause drowsiness.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
COMPARE TO Claritin® 24 Hour active ingredient†
All Day Allergy Relief
LORATADINE TABLETS, 10mg
Antihistamine
Non-Drowsy*
Indoor & Outdoor Allergies
24 hour relief of:
- Sneezing
- Runny Nose
- Itchy, watery eyes
- Itchy Throat or Nose
Gluten-free
TABLETS
*When taken as directed. See Drug Facts panel.
*This product is not manufactured or distributed by Bayer Healthcare LLC, distributor of Claritin® 24 Hour.
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 94566-0009
- Package Label
-
INGREDIENTS AND APPEARANCE
ALL DAY ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-914 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 10 mg Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B) Product Characteristics Color white Score no score Shape ROUND Size 6mm Flavor Imprint Code 439 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21130-914-10 10 in 1 CARTON 03/31/2023 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:21130-914-60 1 in 1 BOX 03/31/2023 2 60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:21130-914-12 1 in 1 BOX 03/31/2023 3 120 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 ANDA075209 03/31/2023 Labeler - Safeway, Inc. (009137209)