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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bubble Fade Away Acne Spot Treatment
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOYL PEROXIDE | 50 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W9WZN9A0GM |
| Rxcui | 106309 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83509-003-01 | Bubble Fade Away Acne Spot Treatment | 1 in 1 CARTON | EMULSION | 1 | | 1 |
| 83509-003-01 | Bubble Fade Away Acne Spot Treatment | 10 mL in 1 TUBE | EMULSION | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83509-003 | BUBBLE FADE AWAY ACNE SPOT TREATMENT (BENZOYL PEROXIDE) EMULSION [BUBBLE BEAUTY] | 1 | Current NDC, 2 package rows | 20250122_2c2dbdc7-8d2e-4ad3-e063-6294a90a6c7e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |