Label: UP AND UP ALLERGY RELIEF- fexofenadine hydrochloride tablet, film coated
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Contains inactivated NDC Code(s)
NDC Code(s): 11673-571-01, 11673-571-22, 11673-571-33, 11673-571-39, view more11673-571-47, 11673-571-49, 11673-571-75, 11673-571-76, 11673-571-87, 11673-571-95 - Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 25, 2022
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- 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
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- do not take more than directed
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- do not take at the same time as aluminum or magnesium antacids
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- do not take with fruit juices (see Directions)
- Directions
- Other information
- Inactive ingredients
- Questions?
- Package/Label Principal Display Panel
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INGREDIENTS AND APPEARANCE
UP AND UP ALLERGY RELIEF
fexofenadine hydrochloride tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-571 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) FERROSOFERRIC OXIDE (UNII: XM0M87F357) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color ORANGE (peach) Score no score Shape ROUND Size 12mm Flavor Imprint Code 93;7253 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-571-39 1 in 1 CARTON 04/13/2011 10/31/2022 1 30 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:11673-571-95 1 in 1 CARTON 11/02/2011 08/18/2016 2 45 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:11673-571-22 15 in 1 CARTON 04/26/2011 02/28/2022 3 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 4 NDC:11673-571-75 1 in 1 CARTON 02/16/2012 05/16/2016 4 90 in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:11673-571-49 1 in 1 CARTON 02/05/2015 08/31/2021 5 40 in 1 BOTTLE; Type 0: Not a Combination Product 6 NDC:11673-571-01 1 in 1 CARTON 03/17/2015 09/30/2022 6 70 in 1 BOTTLE; Type 0: Not a Combination Product 7 NDC:11673-571-76 2 in 1 CARTON 03/16/2015 04/30/2021 7 60 in 1 BOTTLE; Type 0: Not a Combination Product 8 NDC:11673-571-87 1 in 1 CARTON 03/15/2016 07/31/2018 8 300 in 1 BOTTLE; Type 0: Not a Combination Product 9 NDC:11673-571-47 1 in 1 CARTON 01/30/2020 01/31/2022 9 150 in 1 BOTTLE; Type 0: Not a Combination Product 10 NDC:11673-571-33 60 in 1 BOTTLE; Type 0: Not a Combination Product 03/16/2015 04/30/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076447 04/13/2011 Labeler - Target Corporation (006961700)