Label: COMPLETE ALLERGY- diphenhydramine hcl tablet, film coated
- NDC Code(s): 68016-641-00, 68016-641-10, 68016-641-24
- Packager: Chain Drug Consortium
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 21, 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
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
Premier
Value®*COMPARE TO THE ACTIVE INGREDIENT
IN BENADRYL® ALLERGY ULTRATAB® TABLETSComplete Allergy
Diphenhydramine HCl, 25 mg
ANTIHISTAMINEAllergy relief for:
• Sneezing • Runny nose
• Itchy, watery eyes • Itchy throatactual
size24 Tablets
TAMPER EVIDENT: DO NOT USE IF PACKAGE IS
OPENED OR IF BLISTER UNIT IS TORN, BROKEN
OR SHOWS ANY SIGNS OF TAMPERING*This product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the
registered trademark Benadryl® Allergy ULTRATAB® Tablets. 50844 REV0721C32908Distributed By:
Pharmacy Value Alliance, LLC
407 East Lancaster Avenue,
Wayne, PA 19087
If for any reason you are not satisfied with
this product, please return it to the store
where purchased for a full refund.Premier Value 44-329
-
INGREDIENTS AND APPEARANCE
COMPLETE ALLERGY
diphenhydramine hcl tablet, film coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-641 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) D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX) 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) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color pink Score no score Shape OVAL Size 11mm Flavor Imprint Code 44;329 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68016-641-24 2 in 1 CARTON 03/02/1990 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:68016-641-10 1 in 1 CARTON 03/02/1990 2 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:68016-641-00 1 in 1 CARTON 03/02/1990 3 200 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 03/02/1990 Labeler - Chain Drug Consortium (101668460) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(68016-641) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(68016-641) , pack(68016-641) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867894 manufacture(68016-641) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 868734088 manufacture(68016-641) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(68016-641)