Label: CLARITIN- loratadine tablet
- NDC Code(s): 67751-153-02
- Packager: Navajo Manufacturing Company
- This is a repackaged label.
- Source NDC Code(s): 11523-7160
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 1, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- 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?
- Principle Display Panel - 12 Pouch Dispensit
-
INGREDIENTS AND APPEARANCE
CLARITIN
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67751-153(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:67751-153-02 12 in 1 TRAY 12/04/2017 07/01/2025 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA019658 12/04/2017 Labeler - Navajo Manufacturing Company (091917799) Establishment Name Address ID/FEI Business Operations Navajo Manufacturing Company Inc. 136941411 relabel(67751-153) , repack(67751-153)