Label: ALLERGY RELIEF- fexofenadine hydrochloride tablet, film coated
- NDC Code(s): 0363-7011-39
- Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated February 14, 2024
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- Official Label (Printer Friendly)
- 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
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Inactive ingredients
colloidal silicon dioxide, croscarmellose sodium, FD&C blue #2 aluminum lake, iron oxide, lactose monohydrate, magnesium stearate, maltodextrin, microcrystalline cellulose, modified food starch, natural and artificial flavor, peppermint oil, polyethylene glycol, polyvinyl alcohol, pregelatinized starch, propylene glycol, sucralose, talc, titanium dioxide
- Questions or comments?
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Package/Label Principal Display Panel
Walgreens
WALGREENS PHARMACIST RECOMMENDED
Compare to the active ingredient in Allegra® Allergy
Cool Mint Coated Tablets
NON-DROWSY
Allergy Relief
24 HOUR ALLERGY
FEXOFENADINE HYDROCHLORIDE TABLETS, 180 mg / ANTIHISTAMINE
24 Hour
Indoor/Outdoor Allergy Relief
• Sneezing; runny nose; itchy, watery eyes & itchy nose or throat
• Releases a cooling sensation in mouth & throat
30 TABLETS
ACTUAL SIZE
Cool Mint flavor
NOT ACTUAL SIZE
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
fexofenadine hydrochloride tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-7011 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) FD&C BLUE NO. 2 (UNII: L06K8R7DQK) FERRIC OXIDE RED (UNII: 1K09F3G675) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) PEPPERMINT OIL (UNII: AV092KU4JH) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SUCRALOSE (UNII: 96K6UQ3ZD4) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color BLUE Score no score Shape OVAL Size 18mm Flavor MINT Imprint Code L847 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-7011-39 1 in 1 CARTON 02/08/2024 1 30 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA212971 02/08/2024 Labeler - Walgreen Company (008965063)