Active ingredients Purpose

Diphenhydramine HCl – 2% Topical analgesic
Zinc Acetate – 0.1% Skin Protectant

Uses

temporarily relieves itching and pain associated with minor irritations, burns, scrapes, cuts, insect bites and rashes due to poison oak & poison sumac. Dries the oozing and weeping of poison ivy, poison oak & poison sumac.

Warnings
For external use only.
Flammable. Keep away from fire or flame.

Do not use • with any other product containing Diphenhydramine, even onetaken by mouth • on large areas of the body

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 more than 7 days or clear up and occur again within a few days

Keep out of reach of the children
If product is 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 20 o - 25 oC (68 o - 77 oF)

Inactive ingredients

Alcohol, Glycerin, Povidone, Purified Water, Tromethamine

image description

ITCH REL SPR CVS
diphenhydramine hcl 2% zinc acetate 0.1% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69842-845
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	2 g in 100 mL
ZINC ACETATE ANHYDROUS (UNII: H2ZEY72PME) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	0.1 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
POVIDONE (UNII: FZ989GH94E)
WATER (UNII: 059QF0KO0R)
TROMETHAMINE (UNII: 023C2WHX2V)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:69842-845-02	59 mL in 1 CAN; Type 0: Not a Combination Product	02/14/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	02/14/2014

Labeler - CVS (062312574)

Registrant - Product Quest Mfg (927768135)

Name	Address	ID/FEI	Business Operations
Establishment
Product Quest Mfg		927768135	manufacture(69842-845) , label(69842-845)

Drug Facts