ITCH RELIEF- diphenhydramine hcl, zinc acetate spray

Itch Relief by

Drug Labeling and Warnings

Itch Relief by is a Otc medication manufactured, distributed, or labeled by Vi-Jon, LLC. 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 ■ 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, Inc.,

St. Louis, MO 63114

Questions or comments?  1-888-593-0593

295.000/295AB

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)

INGREDIENTS AND APPEARANCE

ITCH RELIEF 
diphenhydramine hcl, zinc acetate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0869-0295
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	18 mg  in 1 mL
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC ACETATE	882 mg  in 1 mL

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: 0869-0295-20	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/14/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	07/14/2010

Labeler - Vi-Jon (790752542)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(0869-0295)