NDC 21091-642-03 - 7 Way De-Wormer
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
- 21091-642
- Requested NDC
- 21091-642-03
- Package NDCs from labels
- 21091-642-01, 21091-642-02, 21091-642-03
- Manufacturer
- Sergeant's Pet Care Products Inc.
- Effective date
- 2026-01-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 7 Way De-Wormer (pyrantel pamoate/praziquantel) Flavored Chewables | Sergeant's Pet Care Products Inc. | 2026-01-21 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21091-642-01 | 7 Way De-Wormer | 2 in 1 PACKAGE | TABLET, CHEWABLE | 2 | 20 | |
| 21091-642-02 | 7 Way De-Wormer | 6 in 1 PACKAGE | TABLET, CHEWABLE | 6 | 20 | |
| 21091-642-03 | 7 Way De-Wormer | 12 in 1 PACKAGE | TABLET, CHEWABLE | 12 | 20 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| PRAZIQUANTEL | ACTIVE INGREDIENT | 6490C9U457 | 7 WAY WORMER (PYRANTEL PAMOATE AND PRAZIQUANTEL) TABLET, CHEWABLE [SERGEANT'S PET CARE PRODUCTS INC.] | 4 | |
| PYRANTEL PAMOATE | ACTIVE INGREDIENT | 81BK194Z5M | 7 WAY WORMER (PYRANTEL PAMOATE AND PRAZIQUANTEL) TABLET, CHEWABLE [SERGEANT'S PET CARE PRODUCTS INC.] | 4 | |
| PRAZIQUANTEL | ACTIVE MOIETY | 6490C9U457 | 7 WAY WORMER (PYRANTEL PAMOATE AND PRAZIQUANTEL) TABLET, CHEWABLE [SERGEANT'S PET CARE PRODUCTS INC.] | 4 | |
| PYRANTEL | ACTIVE MOIETY | 4QIH0N49E7 | 7 WAY WORMER (PYRANTEL PAMOATE AND PRAZIQUANTEL) TABLET, CHEWABLE [SERGEANT'S PET CARE PRODUCTS INC.] | 4 |
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.