Home NDC 42192-143-60 Sodium Sulfacetamide 10% and Sulfur 5% Emollient Foam
Product NDC 42192-143
Requested package NDC 42192-143-60
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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 42192-143 42192-143-60 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 42192-143 SODIUM SULFACETAMIDE 10% AND SULFUR 5% EMOLLIENT FOAM (SULFACETAMIDE SODIUM AND SULFUR) AEROSOL, FOAM [ACELLA PHARMACEUTICALS, LLC] 4 Legacy NDC 20240522_dac8f4e9-7e99-4d87-bb2b-3bf64dc987cd.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 42192-143-60 42192014360 60 g in 1 CAN (42192-143-60) 60 g 2013-04-16 0000-00-00 No No Current