Sodium Sulfacetamide 10% and Sulfur 5% Emollient Foam

Product NDC
42192-143
11-digit product format
421920143
Labeler code
42192
Product ID
42192-143_cf7af88f-1d21-4a1c-b115-3c341c58f9d2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sulfacetamide Sodium and Sulfur
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
Acella Pharmaceuticals, LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2013-06-18
Marketing end
0000-00-00
Substance
SULFACETAMIDE SODIUM; SULFUR
Active strength
10 mg/g; mg/g
Pharmacologic classes
Sulfonamide Antibacterial [EPC],Sulfonamides [CS]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42192-143-01GM - Gram42192-143e3eb1a13-1b77-412d-8e8a-a031eae9fa2b12018-02-20
42192-143-60GM - Gram42192-14369a81b83-603b-4db8-9820-83438de3fce212018-02-20

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42192-143SODIUM SULFACETAMIDE 10% AND SULFUR 5% EMOLLIENT FOAM (SULFACETAMIDE SODIUM AND SULFUR) AEROSOL, FOAM [ACELLA PHARMACEUTICALS, LLC]4Legacy NDC20240522_dac8f4e9-7e99-4d87-bb2b-3bf64dc987cd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
42192-143-0142192014301100 g in 1 CAN (42192-143-01) 100 g2013-06-180000-00-00NoNoCurrent
42192-143-604219201436060 g in 1 CAN (42192-143-60) 60 g2013-04-160000-00-00NoNoCurrent