Home NDC 10742-8397-2 Oxy Face Wash
Product NDC 10742-8397
Requested package NDC 10742-8397-2
11-digit product format 107428397
Labeler code 10742
Product ID 10742-8397_10be40b1-99df-4ee8-8225-f8bc76135ff1
Type HUMAN OTC DRUG
Nonproprietary name benzoyl peroxide
Dosage form LOTION
Route TOPICAL
Labeler The Mentholatum Company
Application part333D
Marketing category OTC MONOGRAPH FINAL
Marketing start 2016-08-01
Marketing end 0000-00-00
Substance BENZOYL PEROXIDE
Active strength 100 mg/mL
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 10742-8397 10742-8397-2 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10742-8397 OXY FACE WASH MAXIMUM ACITON (BENZOYL PEROXIDE) LOTION [THE MENTHOLATUM COMPANY] 3 Legacy NDC 20241219_10be40b1-99df-4ee8-8225-f8bc76135ff1.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 10742-8397-2 10742839702 185 mL in 1 TUBE (10742-8397-2) 185 ml 2016-08-01 0000-00-00 No No Current