Label: ALLERGY RELIEF- diphenhydramine hcl tablet, film coated
- NDC Code(s): 0363-6141-12
- Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 20, 2023
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
Do not use
- to make a child sleepy
- with any other product containing diphenhydramine, even one used on skin
Ask a doctor before use if you have
- a breathing problem such as emphysema or chronic bronchitis
- glaucoma
- difficulty in urination due to enlargement of the prostate gland
- to make a child sleepy
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal display panel
Walgreens
NDC 0363-6141-12
Compare to the active ingredient in
Benadryl® Allergy ULTRATABS®††WALGREENS PHARMACIST RECOMMENDED†
Relieves allergy symptoms
Dye-Free
Allergy ReliefDIPHENHYDRAMINE HCl 25 mg / ANTIHISTAMINE
Mini Tabs
• Relief of runny nose, sneezing,
itchy throat & itchy, watery eyes100
COATED
MINI TABSACTUAL SIZE
TAMPER EVIDENT: DO NOT USE IF
IMPRINTED SAFETY SEAL UNDER
CAP IS BROKEN OR MISSING†Our pharmacists recommend the
Walgreens brand. We invite you to
compare to national brands.††This product is not manufactured or
distributed by Johnson & Johnson
Corporation, owner of the registered
trademark Benadryl® Allergy
ULTRATABS®.DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com
©2021 Walgreen Co.50844 REV0422A61412
Walgreens_44-614
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
diphenhydramine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-6141 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN (UNII: O8232NY3SJ) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STEARIC ACID (UNII: 4ELV7Z65AP) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color white Score no score Shape OVAL Size 11mm Flavor Imprint Code 44;614 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-6141-12 1 in 1 CARTON 09/23/2021 1 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 09/23/2021 Labeler - Walgreen Company (008965063) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(0363-6141) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(0363-6141) , pack(0363-6141) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(0363-6141) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(0363-6141) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(0363-6141)