Label: LORATADINE tablet
-
NDC Code(s):
21130-526-13,
21130-526-31,
21130-526-38,
21130-526-43, view more21130-526-69
- Packager: SAFEWAY INC.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 21, 2021
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- Download DRUG LABEL INFO: PDF XML
- 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 - 10 mg Tablet Bottle Carton
NDC 21130-526-38
Signature
care™
Quality Guaranteed24 HOUR | ORIGINAL PRESCRIPTION STRENGTH
Allergy Relief
Loratadine Tablets, USP 10 mg
AntihistamineCompare to
Claritin®
active ingredient†- •
- Non-drowsy*
- •
- Relief of:
Sneezing; runny nose;
itchy, watery eyes;
itchy throat or nose
*When taken as directed. See Drug Facts Panel.
Actual Size
365 TABLETS
VALUE PACK
-
INGREDIENTS AND APPEARANCE
LORATADINE
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-526 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 STARCH, CORN (UNII: O8232NY3SJ) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color white (White to Off-White) Score no score Shape ROUND Size 6mm Flavor Imprint Code RX526 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21130-526-69 1 in 1 CARTON 06/06/2009 1 10 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:21130-526-31 3 in 1 CARTON 06/06/2009 2 10 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:21130-526-43 1 in 1 CARTON 06/06/2009 3 45 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:21130-526-13 1 in 1 CARTON 06/06/2009 4 120 in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:21130-526-38 1 in 1 CARTON 06/06/2009 5 365 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076134 06/06/2009 Labeler - SAFEWAY INC. (009137209) Establishment Name Address ID/FEI Business Operations Ohm Laboratories Inc. 051565745 MANUFACTURE(21130-526)