Home NDC 24286-1525-4 De La Cruz Sulfur Acne Medication
Product NDC 24286-1525
Requested package NDC 24286-1525-4
11-digit product format 242861525
Labeler code 24286
Product ID 24286-1525_d282404b-2979-316d-e053-2995a90aea2c
Type HUMAN OTC DRUG
Nonproprietary name SULFUR
Dosage form OINTMENT
Route TOPICAL
Labeler DLC Laboratories, Inc.
Application part333D
Marketing category OTC MONOGRAPH FINAL
Marketing start 2014-08-11
Marketing end 0000-00-00
Substance SULFUR
Active strength 10 g/100g
NDC exclude flag No
Listing certified through 2022-12-31
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 · 2 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 24286-1525 24286-1525-4 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 24286-1525 24286-1525-4 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 24286-1525-4 24286152504 6 g in 1 JAR (24286-1525-4) 6 g 2015-03-17 0000-00-00 No No Current