DG ANTI-ITCH- diphenhydramine hydrochloride and zinc acetate cream 
Dollar General

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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DG™ Anti-Itch
Anti-Itch Cream

Drug Facts

Active ingredientsPurposes
Diphenhydramine hydrochloride 2%Topical analgesic
Zinc acetate 0.1%Skin protectant

Uses

Temporarily relieves pain and itching associated with:

Dries the oozing and weeping of poison ivy, poison oak and poison sumac

Warnings

For external use only.

Avoid contact with eyes.

Do Not Use

  • more than directed
  • on large areas of the body
  • with any 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 or does not improve within 7 days
  • symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.

Directions

Other information

Inactive ingredients

cetearyl alcohol (and) polysorbate 60, DMDM hydantoin, glyceryl stearate, isopropyl myristate, mineral oil, phenoxy ethenol, purified water, sodium benzoate

Questions or comments?

1-888-309-9030

DISTRIBUTED BY OLD
EAST MAIN CO.,
100 MISSION RIDGE
GOODLETTSVILLE, TN
37072

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton

DG™|health

NDC 55910-344-24

Compare to
active
ingredients
of Benadryl®
Extra
Strength
Cream*

Extra Strength
Anti-Itch
Cream
Topical Analgesic
and Skin Protectant

Relieves Itches
From Insect Bites
& Skin Irritations

NET WT 1 OZ (28 g)

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton
DG ANTI-ITCH 
diphenhydramine hydrochloride and zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-344
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 acetate0.1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
polysorbate 60 (UNII: CAL22UVI4M)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
mineral oil (UNII: T5L8T28FGP)  
Sodium Benzoate (UNII: OJ245FE5EU)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55910-344-241 in 1 CARTON10/19/2017
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 - Dollar General (068331990)
Establishment
NameAddressID/FEIBusiness Operations
Natureplex LLC062808196MANUFACTURE(55910-344)

Revised: 12/2022
Document Id: fb243550-4a96-406d-8002-a541b1913381
Set id: 6be1c137-3c40-429f-b588-189db2cf46d7
Version: 3
Effective Time: 20221206
 
Dollar General