NDC 61841-180 - Ortizol Otic Solution
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
- 61841-180
- Package NDCs from labels
- 61841-180-05
- Manufacturer
- Bayer HealthCare LLC, Consumer Care
- Effective date
- 2015-02-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ortizol Otic Solution - Bayer HealthCare LLC, Consumer Care | Bayer HealthCare LLC, Consumer Care | 2015-02-05 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 61841-180-05 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-2dc1-f424-e053-dadaa90a57ce | Ortizol-Otic Solution |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61841-180-05 | OrtizolOtic Solution | 15 mL in 1 BOTTLE, DROPPER | LIQUID | 15 | 1 | |
| 61841-180-05 | OrtizolOtic Solution | 1 in 1 CARTON | LIQUID | 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.