FDA.reportPublic FDA data

Micronized Benzoyl Peroxide Treatment

Product NDC
58400-002
11-digit product format
584000002
Labeler code
58400
Product ID
58400-002_808d5869-24f5-4545-81cc-a4ea719e6601
Type
HUMAN OTC DRUG
Nonproprietary name
Benzoyl Peroxide
Dosage form
GEL
Route
TOPICAL
Labeler
Pharmco Laboratories Inc.
Application
part333D
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2012-06-01
Marketing end
0000-00-00
Substance
BENZOYL PEROXIDE
Active strength
50 mg/g
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58400-002-012024-12-23C16284748780-19d75b9d0-2cc5-f424-e053-dadaa90a57cee80fc706-62c7-497b-af15-20246f17228f
58400-002-022024-12-23C16284748780-19d75b9d0-2cc5-f424-e053-dadaa90a57cee80fc706-62c7-497b-af15-20246f17228f
58400-002-012020-01-31C16284748780-19d75b9d0-2cc5-f424-e053-dadaa90a57cee80fc706-62c7-497b-af15-20246f17228f
58400-002-022020-01-31C16284748780-19d75b9d0-2cc5-f424-e053-dadaa90a57cee80fc706-62c7-497b-af15-20246f17228f