Belli Acne Control Spot Treatment
- Product NDC
- 42281-001
- 11-digit product format
- 422810001
- Labeler code
- 42281
- Product ID
- 42281-001_2cdcb7de-ce78-3d94-e063-6394a90a8bec
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SULFUR
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- BODY HALO LLC
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-01-02
- Substance
- SULFUR
- Active strength
- 30 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
- Belli Acne Control Spot Treatment
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SULFUR | 30 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 70FD1KFU70 |
| Rxcui | 199632 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42281-001-00 | Belli Acne Control Spot Treatment | 1 in 1 CARTON | CREAM | 1 | | 8 |
| 42281-001-00 | Belli Acne Control Spot Treatment | 14.75 mL in 1 TUBE | CREAM | 14.75 | | 8 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42281-001 | BELLI ACNE CONTROL SPOT TREATMENT (SULFUR) CREAM [BODY HALO LLC] | 8 | Current NDC, Legacy NDC, 2 package rows | 20250130_da979b69-1e4c-4e2b-82c3-0f155e978652.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42281-001-00 | 42281000100 | 1 TUBE in 1 CARTON (42281-001-00) / 14.75 mL in 1 TUBE | 1 tube | 2022-02-01 | 0000-00-00 | No | No | Current |