Label: ALLERGY RELIEF- diphenhydramine hcl tablet, film coated
- NDC Code(s): 41250-614-12
- Packager: Meijer Distribution Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 25, 2023
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
-
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
- difficulty in urination due to enlargement of the prostate gland
- glaucoma
- to make a child sleepy
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal display panel
meijer®
NDC 41250-614-12
Compare to Benadryl®
Allergy ULTRATABS®
active ingredient*DYE FREE
allergy reliefDiphenhydramine HCl 25 mg | Antihistamine
Relief for • Sneezing • Runny Nose • Itchy Throat • Itchy, Watery Eyes
100 Tablets
Actual
SizeTAMPER EVIDENT: DO NOT USE IF
IMPRINTED SAFETY SEAL UNDER
CAP IS BROKEN OR MISSING*This product is not manufactured or distributed by
Johnson & Johnson Corporation, owner of the
registered trademark Benadryl® Allergy
ULTRATABS®. 50844 REV0422B61412DIST. BY MEIJER
DISTRIBUTION, INC.
GRAND RAPIDS, MI 49544
www.meijer.comOUR QUALITY
GUARANTEE
WWW.MEIJER.COM/SATISFACTION
The Meijer FamilyMeijer 44-614
-
INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
diphenhydramine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-614 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:41250-614-12 1 in 1 CARTON 02/07/2013 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 02/07/2013 Labeler - Meijer Distribution Inc (006959555) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(41250-614) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(41250-614) , pack(41250-614) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(41250-614) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(41250-614) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(41250-614)