NDC 68682-923 - Erythromycin and Benzoyl Peroxide
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
- 68682-923
- Package NDCs from labels
- 68682-923-23
- Manufacturer
- Oceanside Pharmaceuticals | Bausch Health Companies Inc
- Effective date
- 2019-06-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Erythromycin - Oceanside Pharmaceuticals | Bausch Health Companies Inc | Oceanside Pharmaceuticals | Bausch Health Companies Inc | 2019-06-03 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68682-923-23 | Erythromycin and Benzoyl Peroxide | 20 g in 1 JAR | GEL | 20 g | 50 mg in 1g | 9 |
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.