Label: FEXOFENADINE HCL tablet, film coated
- NDC Code(s): 70677-1239-1
- Packager: Strategic Sourcing Services, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 19, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient (in each tablet)Fexofenadine HCl 180 mg
- Purpose Antihistamine
- Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • sneezing • itchy, watery eyes • itching of the nose or throat
- Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
- 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)
- Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.
- If pregnant or breast-feeding,ask a health professional before use.
- Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
- Directions adults and children 12 years and over : take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours - children under 12 years of age : do not use - adults 65 years of age and older : ask a doctor - consumers with kidney disease : ask a doctor
- Other Information • store between 20º and 25ºC (68º and 77ºF) • protect from excessive moisture
- Inactive ingredients colloidal anhydrous silica, colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide red, iron oxide yellow, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch, purified water, titanium dioxide
- Questions or comments? 833-358-6431
- Package and principle display
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INGREDIENTS AND APPEARANCE
FEXOFENADINE HCL
fexofenadine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70677-1239 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) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE (UNII: FZ989GH94E) STARCH, CORN (UNII: O8232NY3SJ) WATER (UNII: 059QF0KO0R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color orange (ORANGE (PEACH)) Score no score Shape CAPSULE Size 17mm Flavor Imprint Code 180 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70677-1239-1 100 in 1 BOTTLE; Type 0: Not a Combination Product 02/22/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA210137 02/22/2024 Labeler - Strategic Sourcing Services, LLC (116956644)
