NDC 65517-0021 - Ready Care XL Kit
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
- 65517-0021
- Package NDCs from labels
- 65517-0021-1
- Manufacturer
- Dukal Corporation
- Effective date
- 2010-11-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ready Care XL Kit - Dukal Corporation | Dukal Corporation | 2010-11-03 | MEDICAL DEVICE |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 47682-088-99 | Ready Care XL Kit | 2 in 1 PACKET | TABLET, CHEWABLE | 6 | 420 mg | 4 |
| 47682-116-99 | Ready Care XL Kit | 2 in 1 PACKET | TABLET, FILM COATED | 6 | 325 mg | 4 |
| 47682-145-99 | Ready Care XL Kit | 2 in 1 PACKET | TABLET, FILM COATED | 6 | 325 mg | 4 |
| 59898-740-01 | Ready Care XL Kit | 0.9 g in 1 PACKET | OINTMENT | 5.4 g | 3.5 mg in 1g | 4 |
| 59898-902-01 | Ready Care XL Kit | 0.9 g in 1 PACKET | CREAM | 5.4 g | 0.13 g in 100g | 4 |
| 65517-0001-1 | Ready Care XL Kit | 0.4 mL in 1 POUCH | SWAB | 8.0 mL | 0.70 mL in 1.0mL | 4 |
| 65517-0004-1 | Ready Care XL Kit | 1.4 mL in 1 POUCH | SWAB | 28.0 mL | 0.00186 mL in 1.4mL | 4 |
| 65517-0021-1 | Ready Care XL Kit | 1 in 1 PACKAGE, COMBINATION | KIT | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 65517-0021 | READY CARE XL KIT (FIRST AID KIT) KIT [DUKAL CORPORATION] | 4 | 8 package rows | 20101104_817e2a80-6d90-42ea-9e85-8daa170f231c.zip |
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.