Micronized Benzoyl Peroxide Treatment
- Product NDC
- 58400-001
- 11-digit product format
- 584000001
- Labeler code
- 58400
- Product ID
- 58400-001_79377e81-d2ea-4df7-af3a-718948fe29df
- 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
- 25 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58400-001-01 | 58400000101 | 59 g in 1 TUBE (58400-001-01) | 59 g | 2012-06-01 | 0000-00-00 | No | No | Current |
| 58400-001-02 | 58400000102 | 3900 g in 1 BOTTLE, PLASTIC (58400-001-02) | 3900 g | 2012-06-01 | 0000-00-00 | No | No | Current |