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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.