NDC 68599-1981-01 - Eye wash
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
- 68599-1981
- Requested NDC
- 68599-1981-01
- Package NDCs from labels
- 68599-1981-1, 68599-1981-4, 68599-1981-01
- Manufacturer
- McKesson | Niagara Pharmaceuticals
- Effective date
- 2022-10-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Eye wash - McKesson | Niagara Pharmaceuticals | McKesson | Niagara Pharmaceuticals | 2022-10-18 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68599-1981-1 | Eye wash | 29.6 mL in 1 BOTTLE, DISPENSING | LIQUID | 29.6 | 4 | |
| 68599-1981-4 | Eye wash | 118.3 mL in 1 BOTTLE, DISPENSING | LIQUID | 118.3 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68599-1981 | EYE WASH (PURIFIED WATER) LIQUID [MCKESSON] | 4 | Current NDC, Legacy NDC, 2 package rows | 20221019_bd089fde-24ba-4de5-e053-2995a90a39bb.zip |
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.