Label: MEIJER CHILDRENS ALLERGY RELIEF BUBBLEGUM FLAVOR- diphenhydramine hcl liquid
- NDC Code(s): 41250-710-08
- Packager: MEIJER DISTRIBUTION INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 1, 2023
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
Do not use
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- to make a child sleepy
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- with any other product containing diphenhydramine, even one used on skin
Ask a doctor before use if the child has
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- a breathing problem such as chronic bronchitis
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- glaucoma
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Directions
- ▪
- find right dose on chart below
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- take every 4 to 6 hours, or as directed by a doctor
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- do not take more than 6 doses in 24 hours
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- 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 doctorchildren 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
meijer®
NDC 41250-710-08
Compare to Children’s Benadryl® Dye-Free active ingredient*
For Ages 6 to 11 Years
CHILDREN’S
allergy liquid
Diphenhydramine HCl
Antihistamine
12.5 mg / 5 mL Oral Solution
Dye-Free | Sugar Free
Bubblegum Flavor
Naturally and artificially flavored
RELIEF OF: Runny Nose, Sneezing, Itchy, Watery Eyes, Itchy Throat or Nose
4 FL OZ (118 mL)
OUR QUALITY GURANTEE
IMPORTANT: Keep this carton for future reference on full labeling.
WWW.MEIJER.COM/SATISFACTION
*This product is not manufactured or distributed by Johnson & Johnson owner of the registered trademark Children’s Benadryl®.
DIST. BY MEIJER DISTRIBUTION, INC.
GRAND RAPIDS, MI 49544
www.meijer.com
DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS TORN OR MISSING
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INGREDIENTS AND APPEARANCE
MEIJER CHILDRENS ALLERGY RELIEF BUBBLEGUM FLAVOR
diphenhydramine hcl liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-710 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 Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-710-08 1 in 1 CARTON 03/07/2017 1 118 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 03/07/2017 Labeler - MEIJER DISTRIBUTION INC (006959555)
