ANTI-ITCH WAL-DRYL- diphenhydramine hcl, zinc acetate spray

Anti-Itch Wal-Dryl by

Drug Labeling and Warnings

Anti-Itch Wal-Dryl by is a Otc medication manufactured, distributed, or labeled by Walgreen's Co, Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Diphenhydramine HCl 2%
Zinc Acetate 0.1%

Purpose

External analgesic
Skin protectant

Uses

for the temporary relief of pain and itching associated with minor skin irritations
dries the oozing and weeping of poison: iv, oak, sumac

Warnings

For external use only

Flammable. Keep away from fire of flame.

Do not use

on large areas of the body

with any other product containing diphenhydramine, even one taken by mouth

Ask a doctor before use

on chicken pox or measles

When using this product

do not get into eyes

Stop use and ask a doctor if

condition worsens or symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

do note use more than directed
adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
children under 2 years of age: ask a doctor

Other information

store at 20⁰ - 25⁰C (68⁰ - 77⁰F)

Inactive ingredients

alcohol, glycerin, povidone, purified water, tris (hydroxymethyl)aminomethane

SPL UNCLASSIFIED SECTION

*Not manufactured or distributed by Johnson + Johnson Consumer Products Company, distributor of Benadryl Spray

Distributed by: Walgreen Co.,
200 Wilmot Rd., Deerfield, IL 60015-4616
100% Satisfaction Guaranteed
www.walgreens.com

PRINCIPAL DISPLAY PANEL

TEAR HERE
Compare to Benadryl Spray active ingredient*
Walgreens Anti-itch Spray
WAL-DRYL
Diphenydramine Hydrochloride2%
Zinc Acetate 0.1%
Topical Analgesic
Skin Protectant
Antihistamine
ITCH RELIEF
2 FL OZ (59 mL)

295.000/295AB

INGREDIENTS AND APPEARANCE

ANTI-ITCH WAL-DRYL 
diphenhydramine hcl, zinc acetate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0295
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	2 kg  in 100 L
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC ACETATE	0.1 kg  in 100 L

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
POVIDONE (UNII: FZ989GH94E)
WATER (UNII: 059QF0KO0R)
TROMETHAMINE (UNII: 023C2WHX2V)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0295-16	0.059 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/08/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	07/08/2011

Labeler - Walgreen's Co (008965063)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(0363-0295)