ANTI-ITCH CREAM- diphenhydramine hydrochloride 2%, zinc acetate 0.1% cream 
Chain Drug Marketing Association Inc.

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Quality Choice Extra Strength Anti-Itch Cream

Active Ingredient

Diphenhydramine Hydrochloride 2%

Purpose

Topical Analgesic

Active Ingredient

Zinc Acetate 0.1%

Purpose

Skin Protectant

For the temporary relief from pain and itching associated with

Warnings

For External Use Only

Do not useon large areas of the body or with any other product containing diphenhydramine, even one taken by mouth

Ask a doctor before use on chicken pox or measles

When using this productavoid contact with eyes

Stop use and ask a doctor if

Stop use and ask a doctor

Keep out of the reach of children

If swallowed, get medical help or contact a Poison Control Center immediately

Directions

Other information

Questions?Call 1-800-935-2362

Inactive Ingredients

Aloe Vera (Aloe Barbadensis) leaf juice, Cetyl alcohol, Glyceryl monostearate, Methylparaben, Mineral Oil, Petrolatum, Polyoxyethylene lauryl ether, Propylene glycol, Propylparaben, Purified Water, Stearic acid

Distributed By

Distributed by CDMA Inc.

Novi, MI 48375

www.qualitychoice.com

Questions: 800-935-2362

This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company owner of the registered trademark Benadryl.

Packaging

94731 QC ANTI ITCH CREAM WITH ALOE 1OZ REV07 042424

ANTI-ITCH CREAM 
diphenhydramine hydrochloride 2%, zinc acetate 0.1% cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-039
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 CATION - UNII:13S1S8SF37) ZINC ACETATE0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
LAURETH-23 (UNII: N72LMW566G)  
WATER (UNII: 059QF0KO0R)  
PETROLATUM (UNII: 4T6H12BN9U)  
MINERAL OIL (UNII: T5L8T28FGP)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83324-039-011 in 1 BOX05/14/2024
128.3 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01705/14/2024
Labeler - Chain Drug Marketing Association Inc. (011920774)
Registrant - Trifecta Pharmaceuticals USA LLC. (079424163)

Revised: 1/2025
Document Id: 2b48d177-e250-2621-e063-6394a90ae278
Set id: 2b48cb2f-e6bf-f9de-e063-6394a90a42d4
Version: 1
Effective Time: 20250109
 
Chain Drug Marketing Association Inc.