Label: CHILDRENS ALLERGY- diphenhydramine hydrochloride liquid
- NDC Code(s): 68016-823-54
- Packager: Chain Drug Consortium, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 30, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Keep out of reach of children
- Uses
- Warnings
- Ask a doctor before use Ask a doctor or pharmacist before use
- When using this product
- Directions
- Other Information
- Inactive ingredients
- Questions or comments?
-
Product Label
NDC 68016-0823-54
*COMPARE TO THE ACTIVE INGREDIENT IN BENADRYL® ALLERGY LIQUID
PREMIER VALUE ®
CHILDREN’S ALLERGY
DIPHENHYDRAMINE
HYDROCHLORIDE
ANTIHISTAMINE
Relieves: Sneezing, Runny Nose, Itchy Watery Eyes, Itchy Throat
Alcohol-Free
Cherry Flavor
4 FL OZ (118 mL)
INDEPENDENTLY TESTED SATISFACTION GUARANTEED PV
If for any reason you are not satisfied with this product, please return it to the store where purchased for a full refund.
DISTRIBUTED BY:
CHAIN DRUG CONSORTIUM
3301 NW BOCA RATON BLVD
SUITE 101, BOCA RATON, FL 33431
BX-005
DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING
*This product is not manufactured or distributed by McNeil-PPC, Inc. distributer of Benadryl® Allergy Liquid.res
-
INGREDIENTS AND APPEARANCE
CHILDRENS ALLERGY
diphenhydramine hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-823 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 12.5 mg in 5 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) POLOXAMER 407 (UNII: TUF2IVW3M2) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM CITRATE (UNII: 1Q73Q2JULR) SUCROSE (UNII: C151H8M554) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68016-823-54 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/11/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M009 09/11/2012 Labeler - Chain Drug Consortium, LLC (101668460) Registrant - AptaPharma Inc. (790523323) Establishment Name Address ID/FEI Business Operations AptaPharma Inc. 790523323 manufacture(68016-823)