DIPHENHYDRAMINE HCL AND ZINC ACETATE- extra strength itch relief spray

Diphenhydramine HCl and Zinc Acetate by

Drug Labeling and Warnings

Diphenhydramine HCl and Zinc Acetate by is a Otc medication manufactured, distributed, or labeled by HEB. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Diphenhydramine HCl 2.0%
Zinc Acetate 0.1%

Purpose

• External Analgesic
• Skin protectant

Uses

for temporary relief of pain and itching associated with:

• minor burns
• sunburns
• minor cuts
• scrapes
• insect bites
• minor skin irritations
• 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.

Flammable:

Keep away from fire or flame. Do not puncture or incinerate. Contents under pressure. Do not store at temperature above 120ºF. Intentional misuse by deliberately concentrating and inhaling contents cans be harmful or fatal.

Do not use

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

Ask a doctor before use

• on chicken pox
• on measles

Stop use and ask doctor if

• condition worsens
• symptoms last more than 7 days or clear up and occur again within a few days

When using this product

• avoid contact with eyes
• use only as directed

Keep out of reach of children.

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

Directions

• 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 between 20° to 25°C (68° to 77°F)

Inactive ingredients

aloe barbadensis leaf juice, glycerin, purified water, SD alcohol 40-B, tromethamine

Questions?

call 1-866-964-0939

Principal Display Panel

HEB

Itch Relief

Extra Strength | Continuous Spray

• Histamine Blocking
• Topical Analgesic
• Skin Protectant

Relieves Itching and pain from insect bites, rashes, poison ivy, sumac and oak.

NET WT 2.7 OZ (76 g)

INGREDIENTS AND APPEARANCE

DIPHENHYDRAMINE HCL AND ZINC ACETATE 
extra strength itch relief spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-526
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	1.52 g  in 76 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC ACETATE	0.076 g  in 76 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
TROMETHAMINE (UNII: 023C2WHX2V)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-526-27	76 g in 1 CAN; Type 0: Not a Combination Product	12/22/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	12/22/2017

Labeler - HEB (007924756)