MedPath

Salicylic Acid

Quality Choice Liquid Corn and Callus Remover

Approved
Approval ID

34188b85-4a14-7565-e063-6394a90a5a10

Product Type

HUMAN OTC DRUG LABEL

Effective Date

May 1, 2025

Manufacturers
FDA

Chain Drug Marketing Association Inc.

DUNS: 011920774

Products 1

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

Liquid Corn and Callus Remover

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code83324-235
Application NumberM030
Product Classification
M
Marketing Category
C200263
G
Generic Name
Liquid Corn and Callus Remover
Product Specifications
Route of AdministrationTOPICAL
Effective DateMay 1, 2025
FDA Product Classification

INGREDIENTS (6)

ALCOHOLInactive
Code: 3K9958V90M
Classification: IACT
ETHYL ETHERInactive
Code: 0F5N573A2Y
Classification: IACT
CASTOR OILInactive
Code: D5340Y2I9G
Classification: IACT
SALICYLIC ACIDActive
Quantity: 170 mg in 1 mL
Code: O414PZ4LPZ
Classification: ACTIB
CAMPHOR (NATURAL)Inactive
Code: N20HL7Q941
Classification: IACT
NITROCELLULOSEInactive
Code: KYR8BR2X6O
Classification: IACT

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