ANTI-ITCH- diphenhydramine hcl, zinc acetate spray

Anti-Itch by

Drug Labeling and Warnings

Anti-Itch by is a Otc medication manufactured, distributed, or labeled by McKesson, Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Diphenhydramine HCL 2%
Zinc acetate .01%

purpose

External analgesic
skin protectant 

Use

• 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 the fire or flame

Do not use

• On large areas of the body
• with any other product containing diphenydramine, 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 to 25⁰ C (68⁰ to 77⁰F)

inactive ingredients

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

Adverse Reactions

Another Quality Product Distributed by McKesson

One Post Street, San Francisco, CA 94104

Money Back Quarantee

Please visit us at www.sunmarkbrand.com

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Compare to Benadryl Spray Active Ingredients

NDC: 49348-992-30

Anti-itch

Spray

relieves itching + pain due

to insect bites, poison ivy, poison oak, poison sumac

For External Use Only

TOPICAL ANALGESIC SKIN PROTECTANT

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

ANTI-ITCH 
diphenhydramine hcl, zinc acetate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49348-992
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 CATION	.882 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
POVIDONE (UNII: FZ989GH94E)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49348-992-30	59 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	06/15/2011

Labeler - McKesson (177667227)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(49348-992)