NDC Code(s) : 0363-0525-56
Packager : Walgreen Company

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Wal-dryl Itch Reliefdiphenhydramine hydrochloride and zinc acetate CREAM
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0363-0525
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DIPHENHYDRAMINE HYDROCHLORIDE(UNII: TC2D6JAD40)
(DIPHENHYDRAMINE - UNII:8GTS82S83M)
DIPHENHYDRAMINE HYDROCHLORIDE2 mg in 1 g
ZINC ACETATE(UNII: FM5526K07A)
(ZINC CATION - UNII:13S1S8SF37)
ZINC CATION1 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
CETYL ALCOHOL(UNII: 936JST6JCN)
METHYLPARABEN(UNII: A2I8C7HI9T)
POLYSORBATE 60(UNII: CAL22UVI4M)
PROPYLENE GLYCOL(UNII: 6DC9Q167V3)
WATER(UNII: 059QF0KO0R)
SORBITAN MONOSTEARATE(UNII: NVZ4I0H58X)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0363-0525-561 in 1 CARTON
128 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part348 01/18/2006

PRINCIPAL DISPLAY PANEL

NDC 0363-0525-56

Walgreens  The Brand America Trusts®

Compare to the active ingredients in BENADRYL ® 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

Wal-Dryl