Sulfur Spot Treatment
- Product NDC
- 85439-0102
- 11-digit product format
- 854390102
- Labeler code
- 85439
- Product ID
- 85439-0102_31e527e0-ce38-e920-e063-6394a90ac827
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sulfur Acne Treatment
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Banuskin, Inc.
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-04-15
- Substance
- SULFUR
- Active strength
- 10 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sulfur Spot Treatment
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SULFUR | 10 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 70FD1KFU70 |
| Rxcui | 315220 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85439-0102-1 | Sulfur Spot Treatment | 15 mL in 1 TUBE | CREAM | 15 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 85439-0102 | SULFUR SPOT TREATMENT (SULFUR ACNE TREATMENT) CREAM [BANUSKIN, INC.] | 1 | Current NDC, 1 package rows | 20250417_31e527e0-ce37-e920-e063-6394a90ac827.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 |
|---|
| 85439-0102-1 | 85439010201 | 15 mL in 1 TUBE (85439-0102-1) | 15 ml | 2025-04-15 | No | No | Historical |