MedPath

Alcortin

Alcortin 1% iodoquinol - 2% hydrocortisone with Aloe

Approved
Approval ID

995ae132-8e37-4fda-b353-ce79ab9d0bf4

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Apr 21, 2010

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.

1% iodoquinol - 2% hydrocortisone

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code68040-702
Product Classification
G
Generic Name
1% iodoquinol - 2% hydrocortisone
Product Specifications
Route of AdministrationTOPICAL
Effective DateApril 20, 2010
FDA Product Classification

INGREDIENTS (2)

HydrocortisoneActive
Quantity: 2 g in 100 g
Code: WI4X0X7BPJ
Classification: ACTIB
IODOQUINOLActive
Quantity: 1 g in 100 g
Code: 63W7IE88K8
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Alcortin - FDA Drug Approval Details