Label: INDOOR OUTDOOR ALLERGY RELIEF- fexofenadine hcl tablet, coated
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NDC Code(s):
0363-0904-05,
0363-0904-15,
0363-0904-30,
0363-0904-45, view more0363-0904-51, 0363-0904-70, 0363-0904-90
- Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 29, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each film-coated 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?
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Principal Display Panel
NON-DROWSY ORIGINAL PRESCRIPTION STRENGTH
Compare to Allegra® Allergy 24 HR active ingredient††
Wal-Fex®
24 HOUR ALLERGY
FEXOFENADINE HCI 180mg / ANTIHISTAMINE
24 HOUR TABLETS
INDOOR & OUTDOOR ALLERGIES
- Relief of runny nose, sneezing, itchy, watery eyes & itchy nose or throat
- Indoor & outdoor allergies
COATED CAPLETS**
(**CAPSULES-SHAPED TABLETS)
††This product is not manufactured or distributed by Chattem Inc., distributor of Allegra® Allergy 24 HR.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
walgreens.com
- Product Label
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INGREDIENTS AND APPEARANCE
INDOOR OUTDOOR ALLERGY RELIEF
fexofenadine hcl tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0904 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) HYPROMELLOSES (UNII: 3NXW29V3WO) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) STARCH, CORN (UNII: O8232NY3SJ) STEARIC ACID (UNII: 4ELV7Z65AP) Product Characteristics Color white Score no score Shape CAPSULE Size 17mm Flavor Imprint Code SG;202 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0904-15 15 in 1 CARTON 08/31/2018 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0363-0904-45 1 in 1 BOX 08/31/2018 2 45 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:0363-0904-70 1 in 1 BOX 08/31/2018 3 70 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 4 NDC:0363-0904-90 1 in 1 BOX 08/31/2018 4 90 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 5 NDC:0363-0904-30 1 in 1 BOX 08/31/2018 5 30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 6 NDC:0363-0904-05 5 in 1 CARTON 08/31/2018 6 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 7 NDC:0363-0904-51 150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/31/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA204507 08/31/2018 Labeler - Walgreens (008965063)