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

ITCH REL SPR by

Drug Labeling and Warnings

ITCH REL SPR by is a Otc medication manufactured, distributed, or labeled by CVS, Product Quest Mfg. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients                          Purpose

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

PURPOSE

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 ​o​C (68 ​o​ - 77 ​o​F)

Inactive ingredients

Alcohol, Glycerin, Povidone, Purified Water, Tromethamine

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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

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

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

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

Labeler - CVS (062312574)

Registrant - Product Quest Mfg (927768135)

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