BenzEFoam Ultra
- Product NDC
- 0187-0201
- 11-digit product format
- 001870201
- Labeler code
- 0187
- Product ID
- 0187-0201_adc4ed21-dfa8-4dad-8e03-e5f07fca03bc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzoyl peroxide
- Dosage form
- AEROSOL
- Route
- TOPICAL
- Labeler
- Bausch Health US, LLC
- Application
- part333D
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-02-06
- Marketing end
- 0000-00-00
- Substance
- BENZOYL PEROXIDE
- Active strength
- 10 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0187-0201-10 | 00187020110 | 1 CAN in 1 CARTON (0187-0201-10) > 100 g in 1 CAN | 1 can | 2020-02-06 | 0000-00-00 | No | No | Current |