warnings
WARNINGS: IF PREGNANT OR BREAST-FEEDING, ask a health professional before use. If symptoms worsen or persist for more than a week, discontinue use and contact a doctor. KEEP OUT OF REACH OF CHILDREN.
OHM Parasites
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
- OHM Parasites
- Generic name
- CHENOPODIUM ANTHELMINTICUM, CINA, CUCURBITA, PEPO, CUPRUM OXYDATUM NIGRUM, FILIX MAS, GRANATUM, KOUSSO, RATANHIA, SANTONINUM, SABADILLA, SPIGELIA, TEUCRIUM MARUM.
- Manufacturer
- OHM PHARMA INC.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 52661b65-ecab-4dc1-9dfd-2fefd9ce24eb
- SPL ID
- d44b89d7-0297-4840-e053-2995a90ac721
- Version
- 4
- Effective date
- 2021-12-29
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:18:48
| 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 | OHM Parasites | openfda.brand_name | |
| generic name | CHENOPODIUM ANTHELMINTICUM, CINA, CUCURBITA, PEPO, CUPRUM OXYDATUM NIGRUM, FILIX MAS, GRANATUM, KOUSSO, RATANHIA, SANTONINUM, SABADILLA, SPIGELIA, TEUCRIUM MARUM. | openfda.generic_name | |
| manufacturer name | OHM PHARMA INC. | openfda.manufacturer_name | |
| ndc | package | 66096-157-05 | openfda.package_ndc |
| ndc | product | 66096-157 | openfda.product_ndc |
| ndc11 | package | 66096015705 | derived:openfda.package_ndc |
| spl id | d44b89d7-0297-4840-e053-2995a90ac721 | id | |
| spl set id | 52661b65-ecab-4dc1-9dfd-2fefd9ce24eb | set_id | |
| unii | 28M1820ACT | openfda.unii | |
| unii | 467D26HS0B | openfda.unii | |
| unii | 82C68SUI26 | openfda.unii | |
| unii | 4H5RSU087I | openfda.unii | |
| unii | V1XJQ704R4 | openfda.unii | |
| unii | 6NAF1689IO | openfda.unii | |
| unii | P29ZH1A35Z | openfda.unii | |
| unii | CLV24I3T1D | openfda.unii | |
| unii | 1VL8J38ERO | openfda.unii | |
| unii | 10464S0TAA | openfda.unii | |
| unii | C0ZK0RRF5X | openfda.unii | |
| unii | GH30P1VXK2 | 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.