ANTI ITCH TOPICAL ANALGESIC- diphenhydramine hydrochloride, zinc acetate cream

Anti itch Topical Analgesic by

Drug Labeling and Warnings

Anti itch Topical Analgesic by is a Otc medication manufactured, distributed, or labeled by Chain Drug Marketing Associations Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients Purpose

Diphenhydramine HCI 2%........................................................Topical analgesic

Zinc acetate, 0.1%.................................................................... Skin protectant

PURPOSE

Uses

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

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use

• with any other product containing diphenhydramine, even one taken by mouth
• on large areas of the body

ASK DOCTOR

Ask a doctor before use

• on chicken pox
• on measles

WHEN USING

When using this product avoid contact with the eyes

STOP USE

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

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away

INDICATIONS & USAGE

Directions

• do not use more than directed
• adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
• children under 12 years of age: consult a doctor

STORAGE AND HANDLING

Other information

• store at 20° to 25°C (68° to 77°F)

INACTIVE INGREDIENT

inactive ingredients

cetyl alcohol, methylparaben, polyoxyl 40 stearate, propylene glycol, propylparaben, purified water, stearyl alcohol

DOSAGE & ADMINISTRATION

DISTRIBUTED BY:

C.D.M.A. INC.

43157 W. NINE MILE

NOVA, MI 48376-0995

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTI ITCH TOPICAL ANALGESIC 
diphenhydramine hydrochloride, zinc acetate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-218
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
CETYL ALCOHOL (UNII: 936JST6JCN)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63868-218-01	1 in 1 BOX	10/12/2016
1		28 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	02/20/2014

Labeler - Chain Drug Marketing Associations Inc (011920774)