ITCH RELIEF CREAM- hydrocortisone cream cream 
Cintas Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

ACTIVE INGREDIENT: HYDROCORTISONE 1%Cream.

Itch Relief Cream

Inactive Ingredients: Benzoic Acid, Chlorphenesin, Citric Acid, Glycerin,Glycerol Monostearate, Methyl Paraben, Mineral Oil,Petrolatum, Phenoxyethanol,Polysorbate 80,Purified Water, Titanium Dioxide,Trisodium Citrate

Keep out of reach of children

USES: For the temporary relief of itching associated with minor, skin irritations and rashes due to eczema, insect bites, poison ivy/oak/sumac, soaps, detergents,cosmetics and jewelry

DIRECTIONS: Adults and children 2years of age and older: apply to affected area and not more than 3 to4 times daity. Children under 2: do not use, consult a doctor.

WARNINGS: For external use only. Avoid contact with eyes. Discontinue use If conditions persist more than 7 days and consult a physician. Do not use on children under 2 years except under the advice and supervision of a physician. Do not use with any other hydrocortisone product unless you have consulted a doctor. Other uses or this product should be only under the advise or supervision of a doctor.

Store at room temperature (do not freeze).

PACKET NOT FOR INDIVIDUAL SALE

Tamper evident: Do not use if package is torn or cut.

Itch Relief Cream

label-01

ITCH RELIEF CREAM 
hydrocortisone cream cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42961-370
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
ANHYDROUS TRISODIUM CITRATE (UNII: RS7A450LGA)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PETROLATUM (UNII: 4T6H12BN9U)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
WATER (UNII: 059QF0KO0R)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
MINERAL OIL (UNII: T5L8T28FGP)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:42961-370-090.9 g in 1 PACKET; Type 0: Not a Combination Product11/29/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34811/29/201612/29/2022
Labeler - Cintas Corporation (056481716)
Registrant - Cintas Corporation (056481716)
Establishment
NameAddressID/FEIBusiness Operations
ULTRAtab Laboratories, Inc. 151051757manufacture(42961-370)

Revised: 12/2022
 
Cintas Corporation