NDC 57561-762 - INTRAUTERINE BOLUS
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
- 57561-762
- Package NDCs from labels
- 57561-762-02
- Manufacturer
- Agri Laboratories, Ltd.
- Effective date
- 2011-03-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| INTRAUTERINE BOLUS Antiseptic and Proteolytic Bolus | Agri Laboratories, Ltd. | 2011-03-08 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57561-762-02 | INTRAUTERINE BOLUS | 50 in 1 JAR | TABLET | 50 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| UREA | ACTIVE INGREDIENT | 8W8T17847W | INTRAUTERINE BOLUS (UREA) TABLET [AGRI LABORATORIES, LTD.] | 1 | |
| UREA | ACTIVE MOIETY | 8W8T17847W | INTRAUTERINE BOLUS (UREA) TABLET [AGRI LABORATORIES, LTD.] | 1 |
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 |
|---|---|---|---|---|---|---|
| Urea 41% | UREA | PureTek Corporation | da5d8eae-8d64-d354-e053-2995a90a7999 | 2022-06-07 | Warnings, Adverse reactions | 8W8T17847W |
| Miracle FootCream Lavender | UREA, GLYCERIN, ALOE, DISODIUM EDTA | Aloe Vera Korea Co.,Ltd. | db520c80-2a2a-5eb1-e053-2995a90a5bb4 | 2022-03-28 | Warnings | 8W8T17847W |
| Miracle FootCream Lemon | UREA, GLYCERIN, ALOE, DISODIUM EDTA | Aloe Vera Korea Co.,Ltd. | db525c63-29fd-2033-e053-2995a90a56b9 | 2022-03-28 | Warnings | 8W8T17847W |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.