FDA.reportPublic FDA data

Sodium Sulfacetamide and Sulfer Emulsion

Product NDC
73352-750
11-digit product format
733520750
Labeler code
73352
Product ID
73352-750_41396a22-cc34-94f2-e063-6294a90afb65
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sodium Sulfacetamide and Sulfer
Dosage form
EMULSION
Route
TOPICAL
Labeler
Trifluent Pharma
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2025-10-04
Substance
SULFACETAMIDE SODIUM; SULFUR
Active strength
100; 10 mg/mL; mg/mL
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
Sodium Sulfacetamide and Sulfer Emulsion
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFACETAMIDE SODIUM100 mg/mL
SULFUR10 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4NRT660KJQInternal UNII lookup
70FD1KFU70Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
999604Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
40601d03-aea0-b0a6-e063-6394a90a1698Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4073022c-5d5d-48f5-82ed-091ad146a4b2Product name120171211
9ffbd0ae-0bce-c086-b707-f0da5f8cd7c5Product name120150828
0304b7d2-7a07-d53b-750f-36012ae6612eProduct name120140508
64c0cc7e-6478-3ca1-8cd7-9a1251d5a3f6Product name120140508
9ae74339-0a3d-82e9-5dd1-88bd2607bd6bProduct name120140508
e44e38a9-2d9e-b0e2-cce9-490554639f3dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73352-750-01Sodium Sulfacetamide and Sulfer Emulsion177 mL in 1 BOTTLEEMULSION1772

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
73352-750-01ML - Milliliter73352-75092c77bf0-fc73-4798-b347-c7ce7feaea2812025-11-13

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sodium Sulfacetamide and Sulfer EmulsionSODIUM SULFACETAMIDE AND SULFERTrifluent Pharma40601d03-aea0-b0a6-e063-6394a90a16982025-10-15Warnings, Adverse reactionsExact identifier
ndc (product): 73352-750

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
999604sulfacetamide sodium 10 % / sulfur 1 % Medicated Liquid SoapPSN40601d03-aea0-b0a6-e063-6394a90a16982
999604sulfacetamide sodium 100 MG/ML / sulfur 10 MG/ML Medicated Liquid SoapSCD40601d03-aea0-b0a6-e063-6394a90a16982
999604sulfacetamide sodium 10 % / sulfur 1 % Medicated Liquid SoapSY40601d03-aea0-b0a6-e063-6394a90a16982

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
73352-750-0173352075001177 mL in 1 BOTTLE (73352-750-01) 177 ml2025-10-04NoNoCurrent