Micronized Benzoyl Peroxide Treatment
- Product NDC
- 58400-003
- 11-digit product format
- 584000003
- Labeler code
- 58400
- Product ID
- 58400-003_f7446e95-362a-4bc0-b4fb-995559ed31fd
- 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
- 100 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 |
|---|
| 58400-003-01 | 58400000301 | 59 g in 1 TUBE (58400-003-01) | 59 g | 2012-06-01 | 0000-00-00 | No | No | Current |
| 58400-003-02 | 58400000302 | 3900 g in 1 BOTTLE, PLASTIC (58400-003-02) | 3900 g | 2012-06-01 | 0000-00-00 | No | No | Current |