Label: FEX-ALLERGY RELIEF- fexofenadine hcl tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 72090-061-90 - Packager: Pioneer Life Sciences, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated September 29, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses:
- Do not use:
- WHEN USING THIS PRODUCT
- ASK A DOCTOR BEFORE USE IF
- STOP USE AND ASK A DOCTOR IF
- If pregnant or breast-feeding
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS OR COMMENTS?
- Keep out of reach of children.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
FEX-ALLERGY RELIEF
fexofenadine hcl tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72090-061 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 MANNITOL (UNII: 3OWL53L36A) STARCH, CORN (UNII: O8232NY3SJ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FD&C RED NO. 40 (UNII: WZB9127XOA) Product Characteristics Color pink Score no score Shape CAPSULE Size 18mm Flavor Imprint Code J;44 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72090-061-90 90 in 1 BOTTLE; Type 0: Not a Combination Product 09/21/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA204097 09/21/2020 Labeler - Pioneer Life Sciences, LLC (014092742)