benzoyl peroxide
- Product NDC
- 72162-2338
- 11-digit product format
- 721622338
- Labeler code
- 72162
- Product ID
- 72162-2338_a2df7901-ab14-4b37-8432-61c6382230b1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZOYL PEROXIDE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2013-01-24
- Substance
- BENZOYL PEROXIDE
- Active strength
- 5 g/100g
- 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 |
|---|
| 72162-2338-2 | 72162233802 | 142 g in 1 BOTTLE (72162-2338-2) | 142 g | 2013-01-24 | No | No | Historical |