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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.