Label: CLARITIN- loratadine tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 73097-005-01, 73097-005-20, 73097-005-25 - Packager: Savings Distributors LLC
- This is a repackaged label.
- Source NDC Code(s): 11523-7160
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated July 10, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient (in each tablet)
- Purpose
- Uses
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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?
- Package Label
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INGREDIENTS AND APPEARANCE
CLARITIN
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73097-005(NDC:11523-7160) 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 Score no score Shape ROUND Size 6mm Flavor Imprint Code 458;Claritin10 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73097-005-01 1 in 1 CARTON 07/03/2019 1 1 in 1 POUCH; Type 0: Not a Combination Product 2 NDC:73097-005-20 20 in 1 CARTON 07/03/2019 2 1 in 1 POUCH; Type 0: Not a Combination Product 3 NDC:73097-005-25 25 in 1 CARTON 07/03/2019 3 1 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA019658 07/03/2019 Labeler - Savings Distributors LLC (010527359)