SALICYLIC ACID
Salicyclic Acid 3% with Benzoic Acid and Oak Bark Extract
Approved
Approval ID
27c9095e-7d3b-46b0-bf34-e34bf815f77d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 10, 2024
Manufacturers
FDA
Trifluent Pharma LLC
DUNS: 117167281
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
SALICYLIC ACID
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code73352-107
Product Classification
G
Generic Name
SALICYLIC ACID
Product Specifications
Route of AdministrationTOPICAL
Effective DateJanuary 10, 2024
FDA Product Classification
INGREDIENTS (1)
SALICYLIC ACIDActive
Quantity: 30 mg in 1 g
Code: O414PZ4LPZ
Classification: ACTIB