GNP EXTRA STRENGTH ANTI-ITCH CREAM- diphenhydramine hydrochloride, zinc acetate cream 
Amerisource Bergen

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Active Ingredients

Diphenhydramine hydrochloride 2%

Zinc acetate 0.1%

Ask Doctor Section

conditions worsen

symptoms last more than 7 days or clear up and occur again within a few days

Do not use section

on chicken pox, poison ivy, sunburn, large areas of the body, broken, blistered, or oozing skin, more often than directed, or with any other product containing diphenhydramine, even one taken by mouth

If swallowed, get medical help or contact a Poison Control Center right away.

For external use only

Directions

do not use more often then directed

adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily

children under 2 years: ask doctor

Uses

temporarily relieves pain and itching due to:

Store at 20C to 25C (68F to 77F)

www.mygnp.com

ceytl alcohol

diazolindinyl urea

methlparaben

polyethylene glycol

monostearate 1000

propylene glycol

propylparaben

purified water

stearyl alcohol

Diphenhydramine hydrochloride...............Topical anagesic

Zinc acetate..............................................Skin protectant

68-258-51v3.0

GNP EXTRA STRENGTH ANTI-ITCH CREAM 
diphenhydramine hydrochloride, zinc acetate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-804
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC ACETATE0.1 g  in 100 g
DIPHENHYDRAMINE HCL (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HCL2 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
WATER (UNII: 059QF0KO0R)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:46122-804-361 in 1 CARTON06/01/2025
11 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01706/01/2025
Labeler - Amerisource Bergen (007914906)
Registrant - Weeks & Leo Co., Inc. (005290028)
Establishment
NameAddressID/FEIBusiness Operations
Weeks & Leo Co., Inc005290028manufacture(46122-804)

Revised: 5/2025
Document Id: 34a66224-ef3d-e36e-e063-6394a90ac99d
Set id: 34a66224-ef3c-e36e-e063-6394a90ac99d
Version: 1
Effective Time: 20250508
 
Amerisource Bergen