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 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

STORAGE AND HANDLING

Other information

• store at room temperature 20-25°C (68-77°F)
• protect from excessive heat (40°C/104°F), humidity, and light

INACTIVE INGREDIENT

inactive ingredients

cetostearyl alcohol, glyceryl stearate/peg-100 stearate, methylparaben, propylene glycol, propylparaben, purified water

DOSAGE & ADMINISTRATION

DISTRIBUTED BY:

C.D.M.A. INC.

43157 W. 9 Mile Road

Novi, MI 48375

www.qualitychoice.com

Made in China

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: 63868-731
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
WATER (UNII: 059QF0KO0R)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63868-731-28	1 in 1 CARTON	04/03/2020
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	04/03/2020

Labeler - Chain Drug Marketing Associations Inc (011920774)