DG HEALTH ANTI ITCH- diphenhydramine hydrochloride, zinc acetate cream 
DOLGENCORP, 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.

----------

Active ingredients                                                                       Purpose

Diphenhydramine Hydrochloride 2% ............................................Topical analgesic

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

Uses

temporarily relieves pain and itching associated with:

Warnings

For external use only

Do not use

Ask a doctor before use

When using this product

Stop use and ask a doctor if

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

Directions

Other information

Inactive ingredients

propylene glycol, cetyl alcohol, polyoxyl 40 stearate, methylparaben, propylparaben, purified water.

Distributed By

Dolgencorp, LLC

100 Mission Ridge

Goodlettsville, TN 37072

Made in Korea

image description

DG HEALTH ANTI ITCH 
diphenhydramine hydrochloride, zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-305
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE20 mg  in 1 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CETYL ALCOHOL (UNII: 936JST6JCN)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55910-305-281 in 1 CARTON09/14/2016
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34805/17/2011
Labeler - DOLGENCORP, INC. (068331990)
Registrant - UNITED EXCHANGE CORP. (840130579)
Establishment
NameAddressID/FEIBusiness Operations
Taiguk Pharm. Co., Ltd._Buyeo branch689060246manufacture(55910-305)

Revised: 9/2016
Document Id: 77803f1a-ff2b-41f2-9a10-b212eb6d4b2d
Set id: 741bf9ef-3450-4248-8c98-637c83965c42
Version: 7
Effective Time: 20160914
 
DOLGENCORP, INC.