DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE - diphenhydramine hydrochloride and zinc acetate cream 
Taro Pharmaceuticals U.S.A., Inc.

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equaline®
anti-itch cream

Drug Facts

Active ingredients	Purpose
Diphenhydramine hydrochloride 2%	Topical analgesic
Zinc acetate 0.1%	Skin protectant

Uses

• temporarily relieves pain and itching associated with:
  • insect bites
  • minor burns
  • sunburn
  • minor skin irritations
  • minor cuts
  • scrapes
  • rashes due to poison ivy, poison oak, and poison sumac
• dries the oozing and weeping of poison ivy, poison oak, and poison 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
• on measles

When using this product

• avoid contact with eyes

Stop use and ask a doctor if

• condition worsens or does not improve within 7 days
• symptoms persist for 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 often 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

• To open: unscrew cap, use pointed end of cap to puncture seal.
• store at room temperature
• see carton or tube crimp for lot number and expiration date

Inactive ingredients

cetyl alcohol, glyceryl stearate, glyceryl stearate/PEG-100 stearate, methylparaben, propylene glycol, propylparaben and purified water

Questions?

Call 1-877-932-7948

DISTRIBUTED BY
SUPERVALU INC.
EDEN PRAIRIE,
MN 55344 USA
MADE IN CANADA

PRINCIPAL DISPLAY PANEL - 28 g Carton

equaline®

compare to Benadryl®
active ingredients*

extra strength
anti-itch cream
2% diphenhydramine HCl

• topical analgesic / antihistamine
• skin protectant

NET WT 1 OZ (28g)

DIPHENHYDRAMINE HYDROCHLORIDE AND ZINC ACETATE  diphenhydramine hydrochloride and zinc acetate   cream

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 51672-2089 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Diphenhydramine hydrochloride (Diphenhydramine) Diphenhydramine hydrochloride 20 mg  in 1 g Zinc acetate (Zinc) Zinc acetate 1 mg  in 1 g

Inactive Ingredients Ingredient Name Strength Cetyl alcohol   Glyceryl Monostearate   Methylparaben   Propylene glycol   Propylparaben   Water

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 51672-2089-2 1 TUBE In 1 CARTON contains a TUBE 1 28 g In 1 TUBE This package is contained within the CARTON (51672-2089-2)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part348	08/07/2009

Labeler - Taro Pharmaceuticals U.S.A., Inc. (145186370)

Establishment
Name	Address	ID/FEI	Operations
Taro Pharmaceuticals Inc.		206263295	MANUFACTURE

Revised: 11/2009Taro Pharmaceuticals U.S.A., Inc.