NDC 85439-0102-01 - Sulfur Spot Treatment
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 85439-0102
- Requested NDC
- 85439-0102-01
- Package NDCs from labels
- 85439-0102-1, 85439-0102-01
- Manufacturer
- Banuskin, Inc.
- Effective date
- 2025-04-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Sulfur Spot Treatment | Banuskin, Inc. | 2025-04-03 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| 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 | 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 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.