MAXIMUM STRENGTH HYDROCORTISONE ANTI-ITCH- hydrocortisone 1% cream 
Target Corporation

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Target Up &Up Maximum Strength Hydrocortisone 1% Anti-itch Cream 

Drug Facts 

Active Ingredient

Hydrocortisone 1.0%

Purpose

Anti-itch

Uses

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

Warnings

For external use only 

Do not use 

When using this product 

Stop use and ask a doctor if 

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Directions 

For itching of skin irritation, inflammation, and rashes:

 For external anal and genital itching, adults:

Other information 

store at a controlled room temperature 20 - 25ºC (68 - 77ºF).

Inactive Ingredients:

 Aloe Barbadensis Leaf Juice, Aluminum Sulfate, Beeswax, Calcium Acetate, Cetearyl Alcohol, Dextrin, Glycerin, Maltodextrin, Methylparaben, Mineral Oil, Petrolatum, Propylparaben, Sodium Cetearyl Sulfate, Sodium Lauryl Sulfate, Purified Water

Questions & Comments ? 1-800-910-6874

Principal Display Panel 

Target Up&Up       NDC 11673-890-56

Maxminium Strenght Hydrocortisone Cream 

Hydrocortisone 1%

Anti-itch 

NET WT 2OZ (56g)

TOTAL NET WT 4OZ (112g)

256994 Tube

556994 Carton

MAXIMUM STRENGTH HYDROCORTISONE ANTI-ITCH 
hydrocortisone 1% cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-890
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ALUMINUM SULFATE (UNII: 34S289N54E)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
CALCIUM ACETATE (UNII: Y882YXF34X)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
ICODEXTRIN (UNII: 2NX48Z0A9G)  
GLYCERIN (UNII: PDC6A3C0OX)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MINERAL OIL (UNII: T5L8T28FGP)  
PETROLATUM (UNII: 4T6H12BN9U)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-890-562 in 1 CARTON01/31/2024
156 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 - Target Corporation (006961700)
Registrant - Sheffield Pharmaceuticals LLC (151177797)
Establishment
NameAddressID/FEIBusiness Operations
Sheffield Pharmaceuticals LLC151177797MANUFACTURE(11673-890) , analysis(11673-890)

Revised: 1/2024
Document Id: b627e4d4-8fbe-4bbf-b399-ba2e37f173c7
Set id: 4ff39cb8-3a20-4fe7-9829-1e882a484668
Version: 2
Effective Time: 20240117
 
Target Corporation