ANTI-ITCH WAL-DRYL- diphenhydramine hcl, zinc acetate spray 
Walgreen's Co

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.

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Walgreens 295.000/295AA/AB Anti-Itch Spray

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

*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

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Compare to Benadryl Spray active ingredient

Walgreens Anti-itch Spray

WAL-DRYL

Diphenydramine Hydrochloride2%

Zinc Acetate 0.1%

ITCH RELIEF

2 FL OZ (59 mL)

image description

ANTI-ITCH WAL-DRYL 
diphenhydramine hcl, zinc acetate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0295
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 kg  in 100 L
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE0.1 kg  in 100 L
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
POVIDONE (UNII: FZ989GH94E)  
WATER (UNII: 059QF0KO0R)  
TROMETHAMINE (UNII: 023C2WHX2V)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0295-160.059 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/08/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/08/2011
Labeler - Walgreen's Co (008965063)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(0363-0295)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(0363-0295)

Revised: 12/2022
Document Id: ee0eab5e-9685-4e22-90c3-572b6fd2ccf2
Set id: 02c6e5b4-f0f8-46f4-b078-7ff63b94037b
Version: 12
Effective Time: 20221219
 
Walgreen's Co