OXY
- Product NDC
- 10742-1206
- 11-digit product format
- 107421206
- Labeler code
- 10742
- Product ID
- 10742-1206_292c10d0-9afe-cbea-e063-6294a90aa1fd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzoyl peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- The Mentholatum Company
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-03-31
- Substance
- BENZOYL PEROXIDE
- Active strength
- 100 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- OXY
- Brand name suffix
- Advanced Care Soothing Cream Acne Cleanser
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOYL PEROXIDE | 100 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W9WZN9A0GM |
| Rxcui | 142034 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10742-1206-1 | 10742120601 | 3 g in 1 POUCH (10742-1206-1) | 3 g | 2022-03-31 | 0000-00-00 | No | No | Current |