warnings
WARNINGS In case of overdose, get medical help or contact a poison control center right away. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.
Herkimer Diamond 8125
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
- Herkimer Diamond 8125
- Generic name
- HERKIMER DIAMOND
- Manufacturer
- Professional Complementary Health Formulas
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0de64388-c1ae-44a7-985d-5d46b2c873c7
- SPL ID
- b90f0dc2-9592-4bbe-8ad5-88c3d3512971
- Version
- 2
- Effective date
- 2026-01-08
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:55:00
| 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 | Herkimer Diamond 8125 | openfda.brand_name | |
| generic name | HERKIMER DIAMOND | openfda.generic_name | |
| manufacturer name | Professional Complementary Health Formulas | openfda.manufacturer_name | |
| ndc | package | 63083-8125-2 | openfda.package_ndc |
| ndc | product | 63083-8125 | openfda.product_ndc |
| ndc11 | package | 63083812502 | derived:openfda.package_ndc |
| spl id | b90f0dc2-9592-4bbe-8ad5-88c3d3512971 | id | |
| spl set id | 0de64388-c1ae-44a7-985d-5d46b2c873c7 | set_id | |
| unii | 6GRV67N0U2 | 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.