HYDROCORTISONE- hydrocortisone cream 
Safetec of America, Inc.

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61010-5800,Safetec First Aid 1% Hydrocortisone Cream

Drug Facts

Active ingredient

Hydrocortisone 1.0%

Purpose

Anti-itch

Uses:

Warnings:

  • Do not usefor the treatment of diaper rash
  • in eyes
  • for feminine itching
  • if condition worsens or lasts more than 7 days, or clears up and occurs again within a few days
  • with any other Hydrocortisone product unless you have consulted a doctor

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? 1-800-456-7077

Manufactured by
SAFETEC OF AMERICA, Inc.
Buffalo, NY 14215 . 800-456-7077
www.safetec.com

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL – 0.9g Pouch Label

Safetec

1% Hydrocortisone Cream™

0.9 g (1/32 oz.)

Safetec of America, Inc.

Buffalo, NY 14215

800-456-7077

PRINCIPAL DISPLAY PANEL – 0.9g Pouch Label

PRINCIPAL DISPLAY PANEL – Box Label

NDC 61010-5800-2

Safetec

First Aid

1% Hydrocortisone Cream

For Temporary Relief of

Itching Associated with

Minor Skin Irritations,

Inflammation, or Rashes

Reorder no. 53110

To reorder:

Call: 1-800-456-7077

Fax: 716-895-2969

Online: www.safetec.com

PRINCIPAL DISPLAY PANEL – Box Label

PRINCIPAL DISPLAY PANEL – 10 Packet Box Label

Safetec®

FIRST AID

Hydrocortisone Cream

1% Hydrocortisone for relief from itching,
inflammation, and rashes

10 Packets

Each Packet Net Wt. 0.9g

Made in USA

Reorder no. 53108

PRINCIPAL DISPLAY PANEL – 10 Packet Box Label
HYDROCORTISONE 
hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61010-5800
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)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
STEARETH-20 (UNII: L0Q8IK9E08)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61010-5800-325 in 1 BOX12/15/2010
1NDC:61010-5800-10.9 g in 1 POUCH; Type 0: Not a Combination Product
2NDC:61010-5800-2144 in 1 BOX12/15/2010
2NDC:61010-5800-10.9 g in 1 POUCH; Type 0: Not a Combination Product
3NDC:61010-5800-410 in 1 BOX04/01/2020
3NDC:61010-5800-10.9 g in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01712/15/2010
Labeler - Safetec of America, Inc. (874965262)
Establishment
NameAddressID/FEIBusiness Operations
Safetec of America, Inc.874965262manufacture(61010-5800)

Revised: 2/2024
Document Id: 10d3fc91-82ae-e8eb-e063-6394a90ae87b
Set id: da2b3b2c-11e0-401b-bbd2-d019271d1b3d
Version: 5
Effective Time: 20240207
 
Safetec of America, Inc.