INSTANT ITCH RELIEF CVS- diphenhydramine hci 2.00% zinc acetate 0.10% spray

Instant Itch Relief by

Drug Labeling and Warnings

Instant Itch Relief by is a Otc medication manufactured, distributed, or labeled by CVS, Product Quest Mfg, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Diphenhydramine HCl 2.0%

Zinc Acetate 0.10%

Purpose

Topical analgesic

Skin protectant

Uses

Temporarily relieves pain and itching associated with:

• insect bites
• minor burns
• sunburn
• minor cuts
• scrapes
• minor skin irritations
• rashes due to poison ivy, oak and sumac
• dries the oozing and weeping of poison ivy, oak and sumac

Warnings

For external use only.

Flammable - Do not use while smoking or near heat or flame ​​​​

Do not use

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

Ask a doctor before use

• on chicken pox
• on measles

Stop use and ask a doctor if

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

WHEN USING

When using this product

keep out of eyes
use only as directed.
do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120F

Keep out of reach of children.

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

Directions

• shake well
• 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
• to apply to face, spray into palm of hand and gently apply

Inactive ingredients

Alcohol, Glycerin, Povidone, Purified Water, Tris (Hydroxymethyl) Aminomethane.

PRINCIPAL DISPLAY PANEL

Instant

Itch Relief

Spray

EXTRA STRENGTH

Histamine Blocking

Relieves itching & pain associated with insect bites & rashes due to poison ivy, oak & sumac

NET WT 3 OZ (85 g)

INGREDIENTS AND APPEARANCE

INSTANT ITCH RELIEF  CVS
diphenhydramine hci 2.00% zinc acetate 0.10% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-234
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	2.0 g  in 100 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	.10 g  in 100 g

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: 59779-234-03	85 g in 1 CAN; Type 0: Not a Combination Product	11/13/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	11/13/2014

Labeler - CVS (062312574)

Registrant - Product Quest Mfg, LLC (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg, LLC		927768135	manufacture(59779-234) , label(59779-234)