Cuprum Phosphoricum
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
- Cuprum Phosphoricum
- Generic name
- CUPRUM PHOSPHORICUM
- Manufacturer
- Hahnemann Laboratories, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f166517a-76d4-cc19-e053-2995a90ae4f1
- SPL ID
- f166517a-76d5-cc19-e053-2995a90ae4f1
- Version
- 1
- Effective date
- 2023-01-03
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:49:39
| 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 | Cuprum Phosphoricum | openfda.brand_name | |
| generic name | CUPRUM PHOSPHORICUM | openfda.generic_name | |
| manufacturer name | Hahnemann Laboratories, INC. | openfda.manufacturer_name | |
| ndc | package | 37662-2233-1 | openfda.package_ndc |
| ndc | package | 37662-2229-1 | openfda.package_ndc |
| ndc | package | 37662-2234-1 | openfda.package_ndc |
| ndc | package | 37662-2231-1 | openfda.package_ndc |
| ndc | package | 37662-2232-4 | openfda.package_ndc |
| ndc | package | 37662-2235-3 | openfda.package_ndc |
| ndc | package | 37662-2233-4 | openfda.package_ndc |
| ndc | package | 37662-2230-3 | openfda.package_ndc |
| ndc | package | 37662-2236-1 | openfda.package_ndc |
| ndc | package | 37662-2231-2 | openfda.package_ndc |
| ndc | package | 37662-2232-3 | openfda.package_ndc |
| ndc | package | 37662-2232-1 | openfda.package_ndc |
| ndc | package | 37662-2234-2 | openfda.package_ndc |
| ndc | package | 37662-2231-4 | openfda.package_ndc |
| ndc | package | 37662-2231-3 | openfda.package_ndc |
| ndc | package | 37662-2229-3 | openfda.package_ndc |
| ndc | package | 37662-2235-2 | openfda.package_ndc |
| ndc | package | 37662-2233-2 | openfda.package_ndc |
| ndc | package | 37662-2234-4 | openfda.package_ndc |
| ndc | package | 37662-2232-2 | openfda.package_ndc |
| ndc | package | 37662-2234-3 | openfda.package_ndc |
| ndc | package | 37662-2235-1 | openfda.package_ndc |
| ndc | package | 37662-2230-2 | openfda.package_ndc |
| ndc | package | 37662-2233-3 | openfda.package_ndc |
| ndc | package | 37662-2229-2 | openfda.package_ndc |
| ndc | package | 37662-2230-1 | openfda.package_ndc |
| ndc | package | 37662-2235-4 | openfda.package_ndc |
| ndc | product | 37662-2234 | openfda.product_ndc |
| ndc | product | 37662-2235 | openfda.product_ndc |
| ndc | product | 37662-2232 | openfda.product_ndc |
| ndc | product | 37662-2236 | openfda.product_ndc |
| ndc | product | 37662-2230 | openfda.product_ndc |
| ndc | product | 37662-2229 | openfda.product_ndc |
| ndc | product | 37662-2233 | openfda.product_ndc |
| ndc | product | 37662-2231 | openfda.product_ndc |
| ndc11 | package | 37662223304 | derived:openfda.package_ndc |
| ndc11 | package | 37662223101 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.