Home NDC 57883-404-10 Plexion
Product NDC 57883-404
Requested package NDC 57883-404-10
11-digit product format 578830404
Labeler code 57883
Product ID 57883-404_463d23fc-cb49-0346-e063-6394a90a2df2
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name SULFACETAMIDE SODIUM, SULFUR
Dosage form CLOTH
Route TOPICAL
Labeler Brava Pharmaceuticals, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2005-09-01
Marketing end 2027-07-31
Substance SULFACETAMIDE SODIUM; SULFUR
Active strength 98; 48 mg/g; mg/g
Pharmacologic classes Sulfonamide Antibacterial [EPC], Sulfonamides [CS]
NDC exclude flag No
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Plexion Active Ingredients# Ingredient, Strength table Ingredient Strength SULFACETAMIDE SODIUM 98 mg/g SULFUR 48 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4NRT660KJQ Internal UNII lookup 70FD1KFU70 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1494170 Internal RxNorm lookup 1494827 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 57883-404-01 Plexion 4 g in 1 PACKET CLOTH 4 5 57883-404-10 Plexion 10 in 1 CARTON CLOTH 10 5 57883-404-60 Plexion 60 in 1 CARTON CLOTH 60 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SULFACETAMIDE SODIUM ACTIVE INGREDIENT 4NRT660KJQ PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 SULFUR ACTIVE INGREDIENT 70FD1KFU70 PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 SULFACETAMIDE ACTIVE MOIETY 4965G3J0F5 PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 SULFUR ACTIVE MOIETY 70FD1KFU70 PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 BENZYL ALCOHOL INACTIVE INGREDIENT LKG8494WBH PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 CETYL ALCOHOL INACTIVE INGREDIENT 936JST6JCN PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 GLYCERYL STEARATE SE INACTIVE INGREDIENT FCZ5MH785I PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 MAGNESIUM ALUMINUM SILICATE INACTIVE INGREDIENT 6M3P64V0NC PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 MAGNESIUM SILICATE INACTIVE INGREDIENT 9B9691B2N9 PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 PEG-100 STEARATE INACTIVE INGREDIENT YD01N1999R PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 PHENOXYETHANOL INACTIVE INGREDIENT HIE492ZZ3T PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 SODIUM THIOSULFATE INACTIVE INGREDIENT HX1032V43M PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 STEARYL ALCOHOL INACTIVE INGREDIENT 2KR89I4H1Y PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1 XANTHAN GUM INACTIVE INGREDIENT TTV12P4NEE PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57883-404 PLEXION (SULFACETAMIDE SODIUM, SULFUR) CLOTH [BRAVA PHARMACEUTICALS, LLC] 4 Current NDC, Legacy NDC, 3 package rows 20241213_8211c8ec-b501-4ac6-8185-b4b9758cdc1a.zip
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 57883-404-10 57883040410 10 PACKET in 1 CARTON (57883-404-10) / 4 g in 1 PACKET (57883-404-01) 10 packet 2005-09-01 2027-07-31 Yes No Current