NDC 49825-124-01 - Breakout Control Acne 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
- 49825-124
- Requested NDC
- 49825-124-01
- Package NDCs from labels
- 49825-124-01, 49825-124-02
- Manufacturer
- Bioelements, Inc. | Cosmetic Enterprises Ltd
- Effective date
- 2012-03-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Breakout Control Acne Treatment - Bioelements, Inc. | Cosmetic Enterprises Ltd | Bioelements, Inc. | Cosmetic Enterprises Ltd | 2012-03-27 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49825-124-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-3f0a-f424-e053-dadaa90a57ce | Breakout Control Acne treatment |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 49825-124-01 | Breakout ControlAcne Treatment | 29 mL in 1 JAR | LOTION | 29 | 1 | |
| 49825-124-02 | Breakout ControlAcne Treatment | 1 in 1 BOX | LOTION | 1 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.