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 American Sales Company, Vi-Jon. 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 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 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 - 25⁰C (68⁰ - 77⁰F)

Inactive ingredients

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

SPL UNCLASSIFIED SECTION

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

Distributed by: American Sales Company
4201 Walden Avenue, Lancaster, NY 14086
S+S BRANDS. INC www.Care1.info
Quality guaranteed or your money back

principal display panel

TEAR HERE
Compare to Active Ingredients in Benadryl Spray*
CAREONE ITCH RELIEF SPRAY
SKIN PROTECTANT
TOPICAL ANALGESIC
Relieves itching due to insect bites poison oak or ivy, or other minor skin irritations
2 FL OZ (59 mL)

295.000/295AB

INGREDIENTS AND APPEARANCE

ITCH RELIEF 
diphenhydramine hcl, zinc acetate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 41520-295
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	2 kg  in 100 L
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC ACETATE	0.1 kg  in 100 L

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: 41520-295-16	0.059 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/06/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	10/06/2011

Labeler - American Sales Company (809183973)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(41520-295)