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- Product NDC
- 49967-259
- 11-digit product format
- 499670259
- Labeler code
- 49967
- Product ID
- 49967-259_95fda45d-d41c-48ec-948f-093506bdf16c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salicylic Acid
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- L'Oreal USA Products Inc
- Application
- part333D
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-07-31
- Marketing end
- 2021-07-31
- Substance
- SALICYLIC ACID
- Active strength
- 20 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 49967-259-01 | 49967025901 | 150 mL in 1 TUBE (49967-259-01) | 150 ml | 2018-07-31 | 0000-00-00 | No | No | Current |