HYDROCORTISONE- hydrocortisone cream 
Unifirst First Aid Corporation

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Medi-First 1% hydrocortisone

Drug Facts

Active ingredient

Hydrocortisone 1.0%

Purpose

Anti-itch

Uses

Warnings

For external use only

Do not use

  • for the treatment of diaper rash
  • with anyother Hydrocortisone product unless you have consulted adoctor
  • if you have vaginal discharge, consulkt a doctor

Stop use and ask a doctor if

  • condition worsens or lasts more than 7 days, or clears and occurs again within a few days
  • you begin use of any other Hydrocortisone product unless you have consulted a doctor
  • bleeding occurs

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

emulsifying wax, ethanol, methylparaben, mineral oil, paraffin, petrolatum, propylparaben, purified water, white wax

Questions or Comments? 1-800-634-7680

Medi-First Hydrocortisone Label

MEDI-FIRST®

1% Hydrocortisone Cream

Temporary relief of itching associated with
minor skin irritation, inflammation and rashes

Product # 24369

10 units of 0.9gm (1/32oz) Packets

24369

Medi First® Plus

Hydrocortisone Cream 1%

Temporary releif of itching associated with minor skin irritation, inflamation and rashes

25 units / Net Wt 0.9 g (1/32 oz)

Item #93373

93373 Hydro

HYDROCORTISONE 
hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-211
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
ALCOHOL (UNII: 3K9958V90M)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MINERAL OIL (UNII: T5L8T28FGP)  
PARAFFIN (UNII: I9O0E3H2ZE)  
PETROLATUM (UNII: 4T6H12BN9U)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
WHITE WAX (UNII: 7G1J5DA97F)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-211-7325 in 1 BOX04/15/2013
1NDC:47682-211-990.9 g in 1 POUCH; Type 0: Not a Combination Product
2NDC:47682-211-1210 in 1 BOX04/15/2013
2NDC:47682-211-990.9 g in 1 POUCH; Type 0: Not a Combination Product
3NDC:47682-211-35144 in 1 BOX04/15/2013
3NDC:47682-211-990.9 g in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01704/15/2013
Labeler - Unifirst First Aid Corporation (832947092)

Revised: 1/2024
Document Id: 0f271047-e96e-f466-e063-6294a90a5cc9
Set id: e90df2e5-2ef4-47dd-bd74-be9cea6d9d85
Version: 17
Effective Time: 20240117
 
Unifirst First Aid Corporation