50096-505 NDC - SODIUM SULFACETAMIDE 9.8% AND SULFUR 4.8% (SULFACETAMIDE SODIUM, SULFUR)

Drug Information

Product NDC: 50096-505

Proprietary Name: Sodium Sulfacetamide 9.8% and Sulfur 4.8%

Non Proprietary Name: SULFACETAMIDE SODIUM, SULFUR

Active Ingredient(s):
  • 98 mg/g SULFACETAMIDE SODIUM;
  • 48 mg/g SULFUR


Administration Route(s): TOPICAL

Dosage Form(s): LOTION

Pharmacy Class(es):
  • Sulfonamide Antibacterial [EPC];
  • Sulfonamides [CS]

Labeler Information

Labeler Name: Rosemar Labs, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:9/1/2005

Package Information

No. Package Code Package Description Billing Unit
150096-505-0257 g in 1 BOTTLE, PLASTIC (50096-505-02)GM

NDC Record

Field Name Field Value Definition
PRODUCT NDC50096-505The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMESodium Sulfacetamide 9.8% and Sulfur 4.8%The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMESULFACETAMIDE SODIUM, SULFURThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELOTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE9/1/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMERosemar Labs, LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMESULFACETAMIDE SODIUM; SULFURAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH98; 48 
ACTIVE INGRED UNITmg/g; mg/g 
PHARM CLASSESSulfonamide Antibacterial [EPC], Sulfonamides [CS] 

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This page was last updated on: 2/1/2023