Benzoyl Peroxide
- Product NDC
- 68071-2307
- 11-digit product format
- 680712307
- Labeler code
- 68071
- Product ID
- 68071-2307_1d78819d-c76c-7ba4-e063-6394a90a404d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoyl Peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- M014
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-01-20
- Substance
- BENZOYL PEROXIDE
- Active strength
- 50 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| W9WZN9A0GM | BENZOYL PEROXIDE | 94-36-0 | BENZOYL PEROXIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-2307-5 | 68071230705 | 42.5 mL in 1 TUBE (68071-2307-5) | 42.5 ml | 2020-11-30 | No | No | Historical |