FIRST AID ONLY HYDROCORTISONE 1% ANTI-ITCH- hydrocortisone cream 
Acme United Corporation

----------

First Aid Only Hydocortisone 1% Anti-Itch Cream

ACTIVE INGREDIENT

Hydrocortisone 1%

PURPOSE

Anti-Itch

USES

Uses ▪ temporarily relieves itching associated with minor skin irritations and rashes

▪other uses should be only under the advice and supervision of a doctor

WARNINGS

For external use only.

Do not use

for a diaper rash. Consult a doctor.

When using this product

  • Avoid contact with the eyes
  • Do not begin use of any other Hydrocortisone product unless you have asked a doctor

Stop use and ask a doctor if

▪ condition worsens or symptoms persist for more than 7 days

▪ symptoms clear up and occur again within a few days

Keep out of reach of children.If swallowed get medical help or contact poison control (800-222-1222) right away.

DIRECTIONS

Adults and children 2 years of age and older Apply to affected area not more than 3 to 4 times daily

Children under 2 years of age Do not use, consult a doctor

OTHER INFORMATION

INACTIVE INGREDIENTS

ceteth-20, cetostearyl alcohol, chlorocresol, liquid paraffin, propylene glycol, purified water, soft paraffin

Questions 1.800.835.2263

Carton image Carton Image

FIRST AID ONLY HYDROCORTISONE 1% ANTI-ITCH 
hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-5633(NDC:50382-024)
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
CETETH-20 (UNII: I835H2IHHX)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
MINERAL OIL (UNII: T5L8T28FGP)  
CHLOROCRESOL (UNII: 36W53O7109)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0924-5633-0112 in 1 CARTON08/05/2022
10.9 g in 1 PACKET; Type 0: Not a Combination Product
2NDC:0924-5633-000.9 g in 1 PACKET; Type 0: Not a Combination Product08/05/2022
3NDC:0924-5633-0225 in 1 CARTON08/05/2022
30.9 g in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01708/02/2012
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corpoation045924339relabel(0924-5633) , repack(0924-5633)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation080119599repack(0924-5633) , relabel(0924-5633)

Revised: 11/2024
Document Id: 274ab3c8-05bc-6f35-e063-6294a90a306e
Set id: e5597b11-b08e-99e1-e053-2a95a90a15a5
Version: 2
Effective Time: 20241119
 
Acme United Corporation