NDC 69626-0011 - Easy Gel
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
- 69626-0011
- Package NDCs from labels
- 69626-0011-5
- Manufacturer
- Leosons Overseas Corp | Ultra Seal Corporation
- Effective date
- 2016-12-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Easy Gel - Leosons Overseas Corp | Ultra Seal Corporation | Leosons Overseas Corp | Ultra Seal Corporation | 2016-12-14 | MEDICAL DEVICE |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69626-0011-5 | Easy Gel | 113.4 g in 1 TUBE | GEL | 113.4 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69626-0011 | EASY GEL (STERILE LUBRICATING JELLY) GEL [LEOSONS OVERSEAS CORP] | 1 | 1 package rows | 20161229_2a9a3aba-d3e0-4fd2-a3f7-535d25fba4eb.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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.