- 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
-
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
-
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)