Itch Relief Spray

Itch Relief Spray

Drug Labeling and Warnings

Drug Details

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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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Itch Relief 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: ivy, oak, sumac

Warnings

For external use only

Flammable.  Keep away from fire or 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 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

  • do not 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 to 25⁰ C (68⁰ to 77⁰ F)

Inactive ingredients

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

*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

295.000/295AB

Principal display panel

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 (790752542)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon790752542manufacture(41250-295)

Revised: 11/2018
 
Meijer Distribution, Inc


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