MedPath

Salinocaine

SALINOCAINE OINTMENT

Approved
Approval ID

49d9f83d-3055-f80e-e58a-b6fca192ac8d

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jul 26, 2023

Manufacturers
FDA

Medical Products Laboratories, Inc.

DUNS: 002290302

Products 1

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

salicylic acid and benzocaine

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code10733-415
Product Classification
G
Generic Name
salicylic acid and benzocaine
Product Specifications
Route of AdministrationTOPICAL
Effective DateJuly 26, 2023
FDA Product Classification

INGREDIENTS (5)

PETROLATUMInactive
Code: 4T6H12BN9U
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
BENZALKONIUM CHLORIDEInactive
Code: F5UM2KM3W7
Classification: IACT
SALICYLIC ACIDActive
Quantity: 550 mg in 1 g
Code: O414PZ4LPZ
Classification: ACTIB
BENZOCAINEActive
Quantity: 20 mg in 1 g
Code: U3RSY48JW5
Classification: ACTIB

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