MedPath

Alcortin A

ALCORTIN® A gel

Approved
Approval ID

3f2abee4-2841-4725-8c11-aafb35ba6bee

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 30, 2009

Manufacturers
FDA

Primus Pharmaceuticals

DUNS: 130834745

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

HYDROCORTISONE ACETATE, ALOE VERA LEAF and Iodoquinol

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code68040-705
Product Classification
G
Generic Name
HYDROCORTISONE ACETATE, ALOE VERA LEAF and Iodoquinol
Product Specifications
Route of AdministrationTOPICAL
Effective DateOctober 30, 2009
FDA Product Classification

INGREDIENTS (3)

HYDROCORTISONE ACETATEActive
Quantity: 20 mg in 1 g
Code: 3X7931PO74
Classification: ACTIB
ALOE VERA LEAFActive
Quantity: 10 mg in 1 g
Code: ZY81Z83H0X
Classification: ACTIB
IodoquinolActive
Quantity: 10 mg in 1 g
Code: 63W7IE88K8
Classification: ACTIB

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Alcortin A - FDA Drug Approval Details