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Plexion

PLEXION Cream (sodium sulfacetamide 9.8%, sulfur 4.8%)

Approved
Approval ID

db71ee55-bbdd-0996-e053-2a95a90a5687

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Mar 30, 2022

Manufacturers
FDA

Eckson Labs LLC

DUNS: 078435242

Products 1

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

SULFACETAMIDE SODIUM, SULFUR

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code44118-701
Product Classification
G
Generic Name
SULFACETAMIDE SODIUM, SULFUR
Product Specifications
Route of AdministrationTOPICAL
Effective DateMarch 30, 2022
FDA Product Classification

INGREDIENTS (2)

SULFURActive
Quantity: 48 mg in 1 g
Code: 70FD1KFU70
Classification: ACTIB
SULFACETAMIDE SODIUMActive
Quantity: 98 mg in 1 g
Code: 4NRT660KJQ
Classification: ACTIB

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Plexion - FDA Drug Approval Details