Label: ALLEGRA ALLERGY- fexofenadine hydrochloride tablet, film coated
ALLEGRA ALLERGY, TRAVEL BASIX- fexofenadine hydrochloride tablet, film coated
- NDC Code(s): 66715-6507-2, 66715-9707-1, 66715-9707-2, 66715-9707-8
- Packager: Lil' Drug Store Products, Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 19, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have kidney disease. Your doctor should determine if you need a different dose.
When using this product
- do not take more than directed
- do not take at the same time as aluminum or magnesium antacids
- do not take with fruit juices (see Directions)
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 5 Tablet Blister Pack Carton
- Allegra Allergy, Travel BASIX
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INGREDIENTS AND APPEARANCE
ALLEGRA ALLERGY
fexofenadine hydrochloride tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66715-9707 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V) FEXOFENADINE HYDROCHLORIDE 180 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) STARCH, CORN (UNII: O8232NY3SJ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color orange (Peach) Score no score Shape OVAL Size 17mm Flavor Imprint Code 018;E Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66715-9707-1 1 in 1 CARTON 11/01/2018 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:66715-9707-2 2 in 1 CARTON 11/01/2018 2 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:66715-9707-8 5 in 1 CARTON 11/01/2018 3 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 NDA020872 09/01/2014 ALLEGRA ALLERGY, TRAVEL BASIX
fexofenadine hydrochloride tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66715-6507 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU) (FEXOFENADINE - UNII:E6582LOH6V) FEXOFENADINE HYDROCHLORIDE 180 mg Inactive Ingredients Ingredient Name Strength MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) STARCH, CORN (UNII: O8232NY3SJ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color orange (Peach) Score no score Shape OVAL Size 17mm Flavor Imprint Code 018;E Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66715-6507-2 2 in 1 CARTON 10/11/2022 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 NDA020872 10/11/2022 Labeler - Lil' Drug Store Products, Inc (093103646)