Label: CHILDREN ALLERGY RELIEF BUBBLEGUM FLAVOR- diphenhydramine hcl liquid
- NDC Code(s): 11673-832-04, 11673-832-08
- Packager: TARGET CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 3, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each 5 mL)
- Purpose
- Uses
- Warnings
-
Directions
- find right dose on chart below
- take every 4 to 6 hours, or as directed by a doctor
- do not take more than 6 doses in 24 hours
- mL = milliliter
Age (yr)
Dose (mL)
children under 2 years
do not use
children 2 to 5 years
do not use unless directed by a doctor
children 6 to 11 years
5 mL to 10 mL
Attention:use only enclosed dosing cup designed for use with this product. Do not use any other dosing device.
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal display panel
NDC 11673-832-04
Compare to active ingredient Children’s Benadryl ®Dye-Free*
dye-free
children’s allergy relief
diphenhydramine HCl 12.5 mg,
Antihistamine/5 mL Oral Solution
Sugar free
for relief of:
- Runny Nose
- Sneezing
- Itchy, Watery Eyes
- Itchy Throat or Nose
BUBBLEGUM FLAVOR
Naturally and Artificially Flavored
AGES 6+ YEARS
4 FL OZ (118 mL)
100% satisfaction guaranteed or your money back.
Each year we give 5% of our profit to communities, which add up to more than $4 Million a week. See all the good we do together at Target.com/Community.
*This product is not manufactured or distributed by Johnson & Johnson owner of the registered trademark Children’s Benadryl ®Dye-Free.
094 04 0378 R01 ID205457
Distributed by Target Corporation
Minneapolis, MN 55403
® & © 2019 Target Brands, Inc.
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IMPORTANT: Keep this carton for future reference on full labeling.
DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS TORN OR MISSING
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INGREDIENTS AND APPEARANCE
CHILDREN ALLERGY RELIEF BUBBLEGUM FLAVOR
diphenhydramine hcl liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-832 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) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) GLYCERIN (UNII: PDC6A3C0OX) POTASSIUM CITRATE (UNII: EE90ONI6FF) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color Score Shape Size Flavor BUBBLE GUM (Naturally and Artificially) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-832-04 1 in 1 CARTON 04/17/2019 1 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:11673-832-08 2 in 1 CARTON 05/15/2025 2 118 mL 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 04/17/2019 Labeler - TARGET CORPORATION (006961700)
