warnings
These statements have not been evaluated by the Food and DrugAdministration. This product is not intended to diagnose, treat, cure, or prevent any diseases.
Fenbendazole 222 MG
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Fenbendazole 222 MG
- Generic name
- FENBENDAZOLE 222 MG
- Manufacturer
- B & L Healthcare Products INC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 337c4554-2049-a725-e063-6394a90a66f5
- SPL ID
- 337c4554-204a-a725-e063-6394a90a66f5
- Version
- 1
- Effective date
- 2025-04-23
- Source export date
- 2026-10-12
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:33:19
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Fenbendazole 222 MG | openfda.brand_name | |
| generic name | FENBENDAZOLE 222 MG | openfda.generic_name | |
| manufacturer name | B & L Healthcare Products INC | openfda.manufacturer_name | |
| ndc | package | 85130-100-02 | openfda.package_ndc |
| ndc | package | 85130-100-01 | openfda.package_ndc |
| ndc | product | 85130-100 | openfda.product_ndc |
| ndc11 | package | 85130010001 | derived:openfda.package_ndc |
| ndc11 | package | 85130010002 | derived:openfda.package_ndc |
| spl id | 337c4554-204a-a725-e063-6394a90a66f5 | id | |
| spl set id | 337c4554-2049-a725-e063-6394a90a66f5 | set_id | |
| unii | 621BVT9M36 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.