ITCH STOPPING CREAM- diphenhydramine hydrochloride 2%, zinc acetate 0.1% cream 
Trifecta Pharmaceuticals USA, LLC.

----------

Best Choice Itch Stopping Cream

Active Ingredient

Diphenhydramine Hydrochloride 2%

Purpose

Topical Analgesic

Active Ingredient

Zinc Acetate 0.1%

Purpose

Skin Protectant

Temporarily relieves pain and itching associated with

Warnings

For External Use Only

Do Not Use

Do Not Use on large areas of the body or with any other product containing diphenhydramine, even one taken by mouth.

When Using this product

When Using this Product avoid contact with Eyes

Stop Use and Ask a Doctor If

Stop Use and Ask a Doctor if

Keep out of the reach of children

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

Ask a Doctor before Use

Ask a doctor before use on chicken pox or measles

Directions

Other information

Inactive Ingredients

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

Distributed By:

Proudly Distributed by Associated Wholesale Grocers Inc.

Kansas City, KS. 66106 USA

Questions Call: 1-877-753-3935

Monday-Friday 9AM-5PM EST

This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., owner of the registered trademark Extra Strength Benadryl® Itch Stopping Cream.

00000 Rev0000000000

Packaging

Best Choice Itch Stopping Cream 1oz 040523 CDER

ITCH STOPPING CREAM 
diphenhydramine hydrochloride 2%, zinc acetate 0.1% cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69396-150
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)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69396-150-011 in 1 BOX11/29/2023
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 DrugM01711/29/2023
Labeler - Trifecta Pharmaceuticals USA, LLC. (079424163)

Revised: 2/2024
Document Id: 11368833-d279-8c29-e063-6294a90a3260
Set id: 11368823-d4af-a536-e063-6294a90a7a2e
Version: 1
Effective Time: 20240212
 
Trifecta Pharmaceuticals USA, LLC.