ANTI-ITCH- diphenhydramine hci, zinc acetate spray

Anti-Itch by

Drug Labeling and Warnings

Anti-Itch by is a Otc medication manufactured, distributed, or labeled by Quality Choice, 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

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, rinse with water to remove
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 Denat.
Glycerin
PVP
Tromethamine
Water

Questions? 248-449-9300

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTI-ITCH 
diphenhydramine hci, zinc acetate spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-785
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: 63868-785-03	85 g in 1 CAN; Type 0: Not a Combination Product	04/07/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/07/2014

Labeler - Quality Choice (011920774)

Registrant - Product Quest Mfg, LLC (927768135)

Establishment
Name	Address	ID/FEI	Business Operations
Product Quest Mfg, LLC		927768135	manufacture(63868-785) , label(63868-785)