MedPath

HYDROCORTISONE IODOQUINOL

Hydrocortisone 1%-Iodoquinol 1% Cream

Approved
Approval ID

52633127-7c36-451a-b6de-30a70a367f30

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

May 6, 2020

Manufacturers
FDA

Syntenza Pharmaceuticals LLC

DUNS: 080999747

Products 1

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

HYDROCORTISONE and IODOQUINOL

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code72056-040
Product Classification
G
Generic Name
HYDROCORTISONE and IODOQUINOL
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 6, 2020
FDA Product Classification

INGREDIENTS (5)

HYDROCORTISONEActive
Quantity: 10 mg in 1 g
Code: WI4X0X7BPJ
Classification: ACTIB
IODOQUINOLActive
Quantity: 10 mg in 1 g
Code: 63W7IE88K8
Classification: ACTIB
WaterInactive
Code: 059QF0KO0R
Classification: IACT
Cetyl AlcoholInactive
Code: 936JST6JCN
Classification: IACT
Polysorbate 20Inactive
Code: 7T1F30V5YH
Classification: IACT

MedPath

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

© 2025 MedPath, Inc. All rights reserved.

HYDROCORTISONE IODOQUINOL - FDA Drug Approval Details