Label: CHILDRENS ALLERGY RELIEF- diphenhydramine hcl liquid
- NDC Code(s): 68998-505-24
- Packager: Marc Glassman, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 19, 2025
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- Official Label (Printer Friendly)
- Drug Facts Active ingredient
- Purpose
- Keep out of reach of children.
- Uses
- Warnings
- Ask a doctor before use if the child has
- Ask a doctor or pharmacist before use if the child is
- When using this product
- Directions
- Other Information
- Inactive ingredients
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Marcs Childrens Allergy Relief Product Label
NDC 68998-505-24
Compare to the active ingredient in children's Benadryl® allergy liquid*
Marcs
Children's
Allergy
Relief
Antihistamine
Diphenhydramine HCL
Oral Solution
Relieves:
Sneezing, Runny Nose,
Itchy Watery Eyes,
Itchy Throat
Alcohol-Free
CHERRY FLVOR
4 FL OZ (118 mL)
DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING
* This product is not manufactured or distributed by McNeil-PPC, Inc., distributor of "Children's Benadryl Allergy Liquid."
Distributed By:
Marc Glassman, Inc.
West 130th Street
Cleveland, OH 44130
BX-044
Internal Label - LR-075 Lot: Exp:


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INGREDIENTS AND APPEARANCE
CHILDRENS ALLERGY RELIEF
diphenhydramine hcl liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68998-505 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 ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 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) Product Characteristics Color Score Shape Size Flavor CHERRY (CHERRY) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68998-505-24 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/02/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 12/02/2014 Labeler - Marc Glassman, Inc. (094487477)
