Bubble Fade Away Acne Spot Treatment
- Product NDC
- 83509-003
- 11-digit product format
- 835090003
- Labeler code
- 83509
- Product ID
- 83509-003_2c2dbdc7-8d2d-4ad3-e063-6294a90a6c7e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzoyl Peroxide
- Dosage form
- EMULSION
- Route
- TOPICAL
- Labeler
- BUBBLE BEAUTY
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-12-01
- 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 |
|---|
| 83509-003-01 | 83509000301 | 1 TUBE in 1 CARTON (83509-003-01) / 10 mL in 1 TUBE | 1 tube | 2024-12-01 | No | No | Historical |