EQUATE HYDROCORTIONE- 1% hydrocortisone cream 
Walmart Inc.

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Equate Hydrocortisone Cream 

Drug Fact 

Active Ingredient 

Hydrocortisone Acetate 1%

Purpose 

Anti itch 

Uses

For temporarily relief of itching associated with minor skin irritations, inflammation, and rashes due to:

■ eczema ■ psoriasis ■ poison ivy, oak, sumac ■ insect bites ■ detergents ■ jewelry ■ cosmetics

■ soaps ■ seborrheic dermatitis

Other uses of this product should only be under the advice and supervision of a doctor

Warnings 

For external use only 

Do not use 

When using this product 

Stop use and ask a doctor if 

condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days, and do not begin use of any other hydrocortisone product unless you have asked a doctor

Keep out of the reach of children 

If swallowed get medical help or contact a poison control center (1-800-222-1222) right away. 

Directions 

Other information 

store at a controlled room temperature 20-25°C (68-77 F)

Inactive ingredients 

Cetearyl Alcohol, Petrolatum, Phenoxyethanol, Propylene Glycol, Sodium Lauryl Sulfate, Water (purified)

Principal  Display Panel 1 oz 

Equate          NDC 79903-211-01

Maximum Strength

Hydrocortisone Cream 1%

Paraben free/Anti-itch

NETWT 1 OZ ( 28g)

590081_WAL2302456_Paraben_Free_Hydrocortisone_1oz_Carton

290081_WAL2302457_Paraben_Free_Hydrocortisone_1oz_Tube

EQUATE HYDROCORTIONE 
1% hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-211
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE ACETATE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
PETROLATUM (UNII: 4T6H12BN9U)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:79903-211-011 in 1 CARTON01/31/2024
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 DrugM01701/31/2024
Labeler - Walmart Inc. (051957769)

Revised: 5/2024
Document Id: 5a00543f-e693-494c-8995-05cfccecc664
Set id: 85b7f620-cc95-4333-b124-bbcc8fd5f7eb
Version: 3
Effective Time: 20240508
 
Walmart Inc.