FDA.reportPublic FDA data

Oxy Face Wash

Product NDC
10742-8397
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct10742-8397DDiscontinued by firm2026-10-12
excluded packagepackage10742-839710742-8397-1DDiscontinued by firm2026-10-12
excluded packagepackage10742-839710742-8397-2DDiscontinued by firm2026-10-12

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 · 3 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproduct10742-8397DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage10742-839710742-8397-1DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage10742-839710742-8397-2DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
10742-8397-12023-02-07Drug Facts - Oxy Face Wash Maximum Action
10742-8397-22023-02-07Drug Facts - Oxy Face Wash Maximum Action
10742-8397-12023-01-30Drug Facts - Oxy Face Wash Maximum Action
10742-8397-22023-01-30Drug Facts - Oxy Face Wash Maximum Action

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10742-8397OXY FACE WASH MAXIMUM ACITON (BENZOYL PEROXIDE) LOTION [THE MENTHOLATUM COMPANY]3Legacy NDC20241219_10be40b1-99df-4ee8-8225-f8bc76135ff1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
10742-8397-110742839701147.7 mL in 1 TUBE (10742-8397-1) 147.7 ml2016-08-010000-00-00NoNoCurrent
10742-8397-210742839702185 mL in 1 TUBE (10742-8397-2) 185 ml2016-08-010000-00-00NoNoCurrent