ITCH RELIEF- diphenhydramine hcl, zinc acetate spray 
Vi-Jon, LLC

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Mountain Falls 295.000 295AA-AB

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 ■ insect bites ■ minor skin irritations ■ sunburn
    ■ minor burns ■ minor cuts ■ scrapes ■ rashes due to poison: ■ ivy ■ oak ■ sumac
  • 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 ■ on measles

When using this product

do not get into eyes

Stop use and ask a doctor if

■ condition worsens
■ 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

Adverse Reactions 

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

Manufactured by: Vi-Jon, LLC

St. Louis, MO 63114

Questions or comments?  1-888-593-0593

principal display panel

Mountain Falls

*Compare to Benadryl

Itch Relief Spray

topical analgesic

skin protectant

Made in the USA with US and foreign parts.

2 FL OZ (59 mL)

mm01

ITCH RELIEF 
diphenhydramine hcl, zinc acetate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0869-0295
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:0869-0295-2059 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/14/201006/17/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01707/14/201006/17/2020
Labeler - Vi-Jon, LLC (088520668)
Registrant - Vi-Jon, LLC (088520668)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC790752542manufacture(0869-0295)
Establishment
NameAddressID/FEIBusiness Operations
Vi-Jon, LLC088520668manufacture(0869-0295)

Revised: 1/2024
 
Vi-Jon, LLC