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.
RET Kidney 7005
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
- RET Kidney 7005
- Generic name
- RET KIDNEY
- Manufacturer
- Professional Complementary Health Formulas
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 017f4c37-3eec-4078-9ce6-aca52fd4974d
- SPL ID
- ce57b1da-4d72-4c34-b5d4-ed9c7d3d4c7c
- Version
- 2
- Effective date
- 2026-01-08
- 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 | RET Kidney 7005 | openfda.brand_name | |
| generic name | RET KIDNEY | openfda.generic_name | |
| manufacturer name | Professional Complementary Health Formulas | openfda.manufacturer_name | |
| ndc | package | 63083-7005-1 | openfda.package_ndc |
| ndc | product | 63083-7005 | openfda.product_ndc |
| ndc11 | package | 63083700501 | derived:openfda.package_ndc |
| spl id | ce57b1da-4d72-4c34-b5d4-ed9c7d3d4c7c | id | |
| spl set id | 017f4c37-3eec-4078-9ce6-aca52fd4974d | set_id | |
| unii | 27YLU75U4W | openfda.unii | |
| unii | 192426I5JU | openfda.unii | |
| unii | E934B3V59H | openfda.unii | |
| unii | 2HEM73YI9I | openfda.unii | |
| unii | 5Q01F7TPJJ | openfda.unii | |
| unii | 4QQN74LH4O | openfda.unii | |
| unii | QDL83WN8C2 | openfda.unii | |
| unii | 95IT3W8JZE | openfda.unii | |
| unii | 1NM3M2487K | openfda.unii | |
| unii | 79Y1949PYO | openfda.unii | |
| unii | 2E32821G6I | openfda.unii | |
| unii | C88X29Y479 | openfda.unii | |
| unii | B7862WZ632 | 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.