NDC 76472-2004 - OLLOPETS WORMS
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
- 76472-2004
- Package NDCs from labels
- 76472-2004-1
- Manufacturer
- SEVENE USA
- Effective date
- 2026-02-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OLLOPETS WORMS - SEVENE USA | SEVENE USA | 2026-02-18 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76472-2004-1 | OLLOPETS WORMS | 30 mL in 1 BOTTLE, DROPPER | SOLUTION | 30 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 76472-2004 | OLLOPETS WORMS (ABROTANUM, ARTEMISIA VULGARIS, CINA, FILIX MAS, INDIGO, NATRUM PHOSPHORICUM, SABADILLA, TEUCRIUM MARUM) SOLUTION [SEVENE USA] | 4 | 1 package rows | 20210608_7db182aa-110b-46f4-b775-ecc7bd3d295e.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 |
|---|---|---|---|---|---|---|
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99ed12d2-f323-0840-e053-2a95a90a40ff | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 9a00c4c9-6631-1737-e053-2a95a90a63f5 | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99daf7c7-e61d-1a0e-e053-2995a90a166c | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99db49c7-89cc-4654-e053-2995a90af6d3 | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99ee837b-c8ff-9ca2-e053-2995a90af6f4 | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99eefa29-21f2-7fb9-e053-2995a90afb60 | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99db0b0c-19f6-6472-e053-2995a90ac7b3 | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99eec2ef-e2e5-9ca6-e053-2995a90a71bf | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99eeeff1-75db-5226-e053-2995a90a42ab | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 9a007e04-eaf4-fc06-e053-2995a90a82d2 | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99ebfabe-7c78-1732-e053-2a95a90aaced | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99ef0e70-5722-da4a-e053-2995a90aabc0 | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 9a0032c4-afd5-4eba-e053-2995a90ad301 | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99ee837b-c902-9ca2-e053-2995a90af6f4 | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99eec2ef-e2ea-9ca6-e053-2995a90a71bf | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 99eee60d-288b-311c-e053-2995a90a850d | 2025-01-09 | QG07G580U0 | |
| Abrotanum | ABROTANUM | Hahnemann Laboratories, Inc. | 9a00719d-eaf6-d8c3-e053-2995a90ac960 | 2025-01-09 | QG07G580U0 | |
| STERILE WATER | STERILE WATER | HF Acquisition Co. LLC, DBA HealthFirst | 74ed2a6f-824c-a1ff-e053-2a91aa0a57c0 | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
| STERILE WATER | STERILE WATER | HF Acquisition Co LLC, DBA HealthFirst | 77bd3c0f-f4ab-7cfa-e053-2a91aa0a1b83 | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
| STERILE WATER | STERILE WATER | HF Acquisition Co LLC, DBA HealthFirst | 7610bf80-61b7-982f-e053-2a91aa0ac1bb | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.