FDA.reportPublic FDA data

SODIUM SULFACETAMIDE, SULFUR

Product NDC
87026-203
Requested package NDC
87026-203-16
11-digit product format
870260203
Labeler code
87026
Product ID
87026-203_4ba947e2-c5dc-e7f7-e063-6294a90aea33
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sodium Sulfacetamide 8% Sulfur 4%
Dosage form
LIQUID
Route
TOPICAL
Labeler
Aspen Medical LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2026-02-01
Substance
SULFACETAMIDE SODIUM; SULFUR
Active strength
80; 40 mg/g; mg/g
Pharmacologic classes
Sulfonamide Antibacterial [EPC], Sulfonamides [CS]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SODIUM SULFACETAMIDE, SULFURSODIUM SULFACETAMIDE 8% SULFUR 4%Aspen Medical LLC4ba94e96-b107-77fe-e063-6394a90aa9802026-02-21Warnings, Adverse reactionsExact identifier
ndc (package): 87026-203-16
ndc (product): 87026-203
ndc11 (package): 87026020316

Additional Listing Data#

Finished product
Yes
Brand name base
SODIUM SULFACETAMIDE, SULFUR
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFACETAMIDE SODIUM80 mg/g
SULFUR40 mg/g

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
1010234Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
4ba94e96-b107-77fe-e063-6394a90aa980Available 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
87026-203-16SODIUM SULFACETAMIDE, SULFUR473 g in 1 BOTTLELIQUID4731

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1010234sulfacetamide sodium 8 % / sulfur 4 % Medicated Liquid SoapPSN4ba94e96-b107-77fe-e063-6394a90aa9801
1010234sulfacetamide sodium 80 MG/ML / sulfur 40 MG/ML Medicated Liquid SoapSCD4ba94e96-b107-77fe-e063-6394a90aa9801
1010234sulfacetamide sodium 8 % / sulfur 4 % Medicated Liquid SoapSY4ba94e96-b107-77fe-e063-6394a90aa9801
1010234sulfacetamide sodium 8 % / sulfur 4 % Topical SuspensionSY4ba94e96-b107-77fe-e063-6394a90aa9801

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
87026-203-1687026020316473 g in 1 BOTTLE (87026-203-16) 473 g2026-02-01NoNoCurrent