FDA.reportPublic FDA data

SODIUM SULFACETAMIDE, SULFUR

Product NDC
87026-202
Requested package NDC
87026-202-06
11-digit product format
870260202
Labeler code
87026
Product ID
87026-202_46064e69-cc1a-8cee-e063-6394a90a8d32
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sodium Sulfacetamide 10%, Sulfur 5%
Dosage form
LIQUID
Route
TOPICAL
Labeler
Aspen Medical LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2026-01-01
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
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFACETAMIDE SODIUM100 mg/g
SULFUR50 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
999613Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
46064e69-cc19-8cee-e063-6394a90a8d32Available 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
87026-202-06SODIUM SULFACETAMIDE, SULFUR170 g in 1 BOTTLELIQUID1701
87026-202-12SODIUM SULFACETAMIDE, SULFUR340 g in 1 BOTTLELIQUID3401

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, SULFURSODIUM SULFACETAMIDE 10%, SULFUR 5%Aspen Medical LLC46064e69-cc19-8cee-e063-6394a90a8d322025-12-15Warnings, Adverse reactionsExact identifier
ndc (package): 87026-202-06
ndc (product): 87026-202
ndc11 (package): 87026020206

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
999613sulfacetamide sodium 10 % / sulfur 5 % Medicated Liquid SoapPSN46064e69-cc19-8cee-e063-6394a90a8d321
999613sulfacetamide sodium 100 MG/ML / sulfur 50 MG/ML Medicated Liquid SoapSCD46064e69-cc19-8cee-e063-6394a90a8d321
999613sulfacetamide sodium 10 % / sulfur 5 % Medicated Liquid SoapSY46064e69-cc19-8cee-e063-6394a90a8d321
999613sulfacetamide sodium 10 % / sulfur 5 % Topical CleanserSY46064e69-cc19-8cee-e063-6394a90a8d321

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
87026-202-0687026020206170 g in 1 BOTTLE (87026-202-06) 170 g2026-01-01NoNoCurrent