ITCH RELIEF- diphenhydramine hcl, zinc acetate spray 
Meijer Distribution, Inc

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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Meijer 295.000-295AA-AB Itch Relief Spray

Active ingredients

Diphenhydramine HCL 2%

Zinc acetate 0.1%

Purpose

External analgesic

Skin protectant

Uses

Warnings

For external use only

Flammable.  Keep away from fire or flame.

Do not use

Ask a doctor before use

When using this product

do not get in 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

Other information

store at 20⁰ to 25⁰ C (68⁰ to 77⁰ F)

Inactive ingredients

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

Disclaimer

*This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Benadryl Spray.

Distributed by Meijer Distribution, Inc.

Grand Rapids, MI 49544

www.meijer.com

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TEAR HERE

Meijer

Compare to the active ingredients in Benadryl Spray*

Itch Relief Spray

topical analgesic

skin protectant

Pain & Itch Reliever

2 FL OZ (59 mL)

image description

ITCH RELIEF 
diphenhydramine hcl, zinc acetate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-295
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE18 mg  in 1 mL
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE882 mg  in 1 mL
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:41250-295-2059 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34811/01/2018
Labeler - Meijer Distribution, Inc (006959555)
Registrant - Vi-Jon, LLC (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(41250-295)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(41250-295)

Revised: 4/2022
Document Id: eeaf12a0-d7e5-426e-96c3-407831576cd7
Set id: e11390ec-99a3-4ff1-a3c8-ca909f4f67b5
Version: 10
Effective Time: 20220414
 
Meijer Distribution, Inc