Label: CHILDRENS ALLERGY DYE FREE WAL DRYL- diphenhydramine hydrochloride liquid
- NDC Code(s): 0363-0710-08
- Packager: WALGREEN CO.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each 5 mL)
- Purpose
- Uses
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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 the child has
- •
- a breathing problem such as chronic bronchitis
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- glaucoma
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Directions
- •
- find right dose on chart below
- •
- 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
- •
- 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
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PRINCIPAL DISPLAY PANEL
Walgreens
NDC 0363-0710-08
Compare to Children’s Benadryl ® Dye-Free active ingredient††
children’s ALLERGY Dye-Free Wal-Dryl®
DIPHENHYDRAMINE HCl /ANTIHISTAMINE
12.5 mg/ 5 mL ORAL SOLUTION
DYE & SUGAR FREE
- •
- For the relief of runny nose, itchy throat or nose, sneezing, & itchy, watery eyes
- AGES 6 -11 YEARS
BUBBLE GUM FLAVOR
8 FL OZ (236 mL)
Walgreens
Pharmacist Recommended†
Health expertise you rely on, quality you trust.
†Walgreens Pharmacist Survey
††This product is not manufactured or distributed by Johnson and Johnson owner of the registered trademark Children’s Benadryl® Dye–Free
DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS TORN OR MISSING
IMPORTANT : KEEP THIS CARTON FOR FUTURE REFERENCE ON FULL LABELING
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INGREDIENTS AND APPEARANCE
CHILDRENS ALLERGY DYE FREE WAL DRYL
diphenhydramine hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0710 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 CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) anhydrous citric acid (UNII: XF417D3PSL) 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:0363-0710-08 1 in 1 CARTON 08/31/2017 1 236 mL in 1 BOTTLE; 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 08/31/2017 Labeler - WALGREEN CO. (008965063)
