NDC 72204-903-01 - ERADIKATE ACNE MARK FADING
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
- 72204-903
- Requested NDC
- 72204-903-01
- Package NDCs from labels
- 72204-903-01, 72204-903-02
- Manufacturer
- Rare Beauty Brands Inc.
- Effective date
- 2025-12-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| KATE SOMERVILLE (as PLD) - ERADIKATE ACNE MARK FADING GEL (43479-112) | Rare Beauty Brands Inc. | 2025-12-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72204-903-01 | ERADIKATE ACNE MARK FADING | 30 mL in 1 BOTTLE | GEL | 30 | 8 | |
| 72204-903-02 | ERADIKATE ACNE MARK FADING | 1 in 1 BOX | GEL | 1 | 8 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.