QUALITY CHOICE EXTRA STRENGTH ANTI ITCH - diphenhydramine hydrochloride, zinc acetate cream 
CHAIN DRUG MARKETING ASSOCIATION INC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredients                                                                               Purpose

Diphenhydramine hydrochloride USP, 2%.............................................Antihistamine

Zinc acetate, 0.1%.............................................................................Skin protectant

Uses

Warnings

For external use only

Do not use

When using this product avoid contact with the eyes

Stop use and ask a doctor if condition worsens, or if symptoms persists for more than 7 days, or clear up and occur again within a few days

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

Other information

Inactive ingredients

glycerin, sodium chloride, petrolatum, cetyl alcohol, dimethicone, isopropyl palmitate, distearyldimodium chloride (1-Octadecanaminium, N, N-Dimmethyl-N-Octadecyl-Chloride), methylparaben, propylparaben, purified water, hydroxyethyl cellulose

DISTRIBUTED BY QUALITY CHOICE

NOVI, MI 48376-0995

MADE IN KOREA

QC 94731

www.chaindrug.com

image of carton labelEnter section text here

QUALITY CHOICE EXTRA STRENGTH ANTI ITCH 
diphenhydramine hydrochloride, zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-947
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE2 g  in 100 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC - UNII:J41CSQ7QDS) ZINC ACETATE0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
PETROLATUM (UNII: 4T6H12BN9U)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-947-301 in 1 CARTON
130 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33602/13/2012
Labeler - CHAIN DRUG MARKETING ASSOCIATION INC (011920774)

Revised: 2/2012
Document Id: 53c9d44d-7fd1-4aaa-89d7-2fa8c10e26ad
Set id: 6b99d52d-6e5f-4b5f-beae-bb1107007163
Version: 1
Effective Time: 20120213
 
CHAIN DRUG MARKETING ASSOCIATION INC