Home NDC 24470-942 Plexion
Product NDC 24470-942
11-digit product format 244700942
Labeler code 24470
Product ID 24470-942_399a083d-734f-3e35-e063-6294a90ad8fc
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name SULFACETAMIDE SODIUM, SULFUR
Dosage form CREAM
Route TOPICAL
Labeler Cintex Services, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-07-10
Substance SULFACETAMIDE SODIUM; SULFUR
Active strength 98; 48 mg/g; mg/g
Pharmacologic classes Sulfonamide Antibacterial [EPC], Sulfonamides [CS]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Plexion
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 98 mg/g SULFACETAMIDE SODIUM 48 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 70FD1KFU70 Internal UNII lookup 4NRT660KJQ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1494173 Internal RxNorm lookup 1494826 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 24470-942-02 Plexion 57 g in 1 BOTTLE, PLASTIC CREAM 57 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Plexion SULFACETAMIDE SODIUM, SULFUR Cintex Services, LLC 399a01bb-e454-3e20-e063-6294a90ab17c 2025-07-10 Warnings, Adverse reactions Exact identifier ndc (product): 24470-942
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 24470-942-02 24470094202 57 g in 1 BOTTLE, PLASTIC (24470-942-02) 57 g 2025-07-10 No No Current