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 DOLGENCORP, LLC, 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: ivy, oak, sumac

Warnings

For external use only

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 worses 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

SPL UNCLASSIFIED SECTION

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

DISTRIBUTED BY DOLGENCORP, LLC

100 MISSION RIDE

GOODLETTSVILLE, TTN 37072

principal display panel

TEAR HERE

DG health

Compare to active ingredents in Benadryl Spray

Itch Relief Spray

External Analgesic

Skin Protectant

Relieves itching due to insect bites, poison oak or ivy, or other monor skin irritations

100% Satisfaction Guaranteed! (888)309-9030

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: 55910-295
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: 55910-295-16	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 - DOLGENCORP, LLC (068331990)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(55910-295)