Sodium Sulfacetamide

Product NDC
72162-1665
Requested package NDC
72162-1665-7
11-digit product format
721621665
Labeler code
72162
Product ID
72162-1665_233623bf-3ee7-437d-a8e6-1a71bc16f299
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sodium Sulfacetamide
Dosage form
LIQUID
Route
TOPICAL
Labeler
Bryant Ranch Prepack
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2022-01-15
Substance
SULFACETAMIDE SODIUM
Active strength
100 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
Sodium Sulfacetamide
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SULFACETAMIDE SODIUM100 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

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

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1006107Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
acd3fb4a-558d-4565-84d8-23a0d917eab6Available 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
72162-1665-2Sodium Sulfacetamide355 g in 1 BOTTLELIQUID355100
72162-1665-4Sodium Sulfacetamide480 g in 1 BOTTLELIQUID480100
72162-1665-7Sodium Sulfacetamide177 g in 1 BOTTLELIQUID177100

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1665-2GM - Gram72162-16650c1c2050-0968-49db-adda-60879ca3898c12025-02-10
72162-1665-4GM - Gram72162-166576b2b5a2-c1c9-4657-a046-7662ff3cfd9812025-02-10
72162-1665-7GM - Gram72162-16657e98abd6-1edf-47aa-ad37-981dac3b8a3912025-02-10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-1665SODIUM SULFACETAMIDE LIQUID [BRYANT RANCH PREPACK]100Current NDC, 3 package rows20241228_acd3fb4a-558d-4565-84d8-23a0d917eab6.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
Sodium SulfacetamideSODIUM SULFACETAMIDEBryant Ranch Prepackacd3fb4a-558d-4565-84d8-23a0d917eab62024-12-24WarningsExact identifier
ndc (package): 72162-1665-7
ndc (product): 72162-1665
ndc11 (package): 72162166507

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1006107sulfacetamide sodium 10 % Medicated Liquid SoapPSNacd3fb4a-558d-4565-84d8-23a0d917eab6100
1006107sulfacetamide sodium 100 MG/ML Medicated Liquid SoapSCDacd3fb4a-558d-4565-84d8-23a0d917eab6100
1006107sulfacetamide sodium 10 % Medicated Liquid SoapSYacd3fb4a-558d-4565-84d8-23a0d917eab6100

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-1665-772162166507177 g in 1 BOTTLE (72162-1665-7) 177 g2024-12-24NoNoCurrent