HYDROCORTISONE- hydrocortisone cream 
AKRON PHARMA INC

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MEDPURA
Hydrocortisone Anti-Itch Cream 1%
Maximum Strength

Drug Facts

Active Ingredient

Hydrocortisone 1%

Purpose

Anti-itch

Uses

temporarily relieves 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 Poison Control Center right away (1-800-222-1222).

Directions

for itching of skin irritation, inflammation, and rashes:

for external anal and genital itching, adults:

Other Information

Store at 20-250C (68-770F).

Inactive Ingredients

aloe vera, benzyl alcohol, glyceryl monostearate, mineral oil, PEG-40, PEG-25, propylene glycol, purified water, squalane, stearic acid.

Questions or Comments?

Call toll-free 1-877-225-6999

Manufactured for:

Akron Pharma, Inc.
Fairfield, NJ 07004

www.akronpharma.com

Made in USA

16Oz

1Oz

HYDROCORTISONE 
hydrocortisone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71399-0180
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 mg  in 100 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
MINERAL OIL (UNII: T5L8T28FGP)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
water (UNII: 059QF0KO0R)  
SQUALANE (UNII: GW89575KF9)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71399-0180-1454 g in 1 JAR; Type 0: Not a Combination Product11/05/2021
2NDC:71399-0180-21 in 1 CARTON11/20/2023
228 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01711/05/2021
Labeler - AKRON PHARMA INC (067878881)

Revised: 11/2023
Document Id: f65bd138-874d-4b49-9540-a47188150c3c
Set id: fa956b6a-1712-4f7a-9490-11866dcd17c8
Version: 3
Effective Time: 20231126
 
AKRON PHARMA INC