Label: WAL-DRYL- diphenhydramine hydrochloride and zinc acetate cream
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Contains inactivated NDC Code(s)
NDC Code(s): 0363-0122-01 - Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 27, 2014
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- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- DO NOT USE
- ASK A DOCTOR BEFORE USE
- WHEN USING THIS PRODUCT
- STOP USE AND ASK A DOCTOR IF
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- OTHER INFORMATION
- INACTIVE INGREDIENT
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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC 0363-0525-56
Walgreens The Brand America Trusts®
Compare to the active ingredients inBENADRYL® EXTRA STRENGTH ITCH STOPPING CREAM*
Wal-dryl
Topical Analgesic/Skin Protectant
ITCH RELIEF
MAXIMUM STRENGTH
2% Diphenhydramine Hydrochloride, USP and 0.1% Zinc Acetate, USP
Temporary Relief of Itch and Pain due to
• Insect Bites • Minor Skin Irritations •Rashes from Poison Ivy, Poison Oak or Poison Sumac
PHARMACIST RECOMMENDED
NET WT. 1 OZ (28 g)
05250111F1 VC110348
*This product is not affiliated with, manufactured by, or produced by the makers or owners of Benadryl®.
Made in USA
Distributed by: Walgreen Co.,
200 Wilmot Rd., Deerfield, IL 60015-4616
Quality Guaranteed
100% Satisfaction Guaranteed with all Walgreens Products or Your Money Back. www.walgreeens.com
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INGREDIENTS AND APPEARANCE
WAL-DRYL
diphenhydramine hydrochloride and zinc acetate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0122 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 2 mg in 1 g ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 0.1 mg in 1 g Inactive Ingredients Ingredient Name Strength CARBOMER 940 (UNII: 4Q93RCW27E) CETYL ALCOHOL (UNII: 936JST6JCN) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PARAFFIN (UNII: I9O0E3H2ZE) METHYLPARABEN (UNII: A2I8C7HI9T) POLYSORBATE 60 (UNII: CAL22UVI4M) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) STEARIC ACID (UNII: 4ELV7Z65AP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0122-01 1 in 1 CARTON 1 28 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part348 03/27/2014 Labeler - Walgreen Company (008965063) Registrant - NeoPharm Co., Ltd. (631101883) Establishment Name Address ID/FEI Business Operations NeoPharm Co., Ltd. 631101883 manufacture(0363-0122)