FDA.reportPublic FDA data

SULFACETAMIDE SODIUM, SULFUR

Product NDC
24470-932
11-digit product format
244700932
Labeler code
24470
Product ID
24470-932_0d1f8666-9600-7844-e063-6394a90af412
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
SULFACETAMIDE SODIUM, SULFUR
Dosage form
LOTION
Route
TOPICAL
Labeler
Cintex Services, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2024-01-23
Substance
SULFACETAMIDE SODIUM; SULFUR
Active strength
100; 50 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
SULFACETAMIDE SODIUM, SULFUR
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFUR100 mg/g
SULFACETAMIDE SODIUM50 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

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

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1005856Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
0d1f8666-95ff-7844-e063-6394a90af412Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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
24470-932-01SULFACETAMIDE SODIUM, SULFUR1 in 1 CARTONLOTION11
24470-932-01SULFACETAMIDE SODIUM, SULFUR25 g in 1 BOTTLE, PLASTICLOTION251

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
24470-932-01GM - Gram24470-9326bfe8cfb-7fc1-4796-b6de-7181915065df12024-03-12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24470-932SULFACETAMIDE SODIUM, SULFUR LOTION [CINTEX SERVICES, LLC]1Current NDC, 2 package rows20240124_0d1f8666-95ff-7844-e063-6394a90af412.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SULFACETAMIDE SODIUM, SULFURSULFACETAMIDE SODIUM, SULFURCintex Services, LLC0d1f8666-95ff-7844-e063-6394a90af4122024-01-23Warnings, Adverse reactionsExact identifier
ndc (product): 24470-932

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1005856sulfacetamide sodium 10 % / sulfur 5 % Topical LotionPSN0d1f8666-95ff-7844-e063-6394a90af4121
1005856sulfacetamide sodium 100 MG/ML / sulfur 50 MG/ML Topical LotionSCD0d1f8666-95ff-7844-e063-6394a90af4121
1005856sulfacetamide sodium 10 % / sulfur 5 % Topical LotionSY0d1f8666-95ff-7844-e063-6394a90af4121
1005856sulfacetamide sodium 10 % / sulfur 5 % Topical SuspensionSY0d1f8666-95ff-7844-e063-6394a90af4121

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
24470-932-01244700932011 BOTTLE, PLASTIC in 1 CARTON (24470-932-01) / 25 g in 1 BOTTLE, PLASTIC2024-01-23NoNoCurrent