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 Bladder 7006
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 Bladder 7006
- Generic name
- RET BLADDER
- Manufacturer
- Professional Complementary Health Formulas
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f1d354e7-3d72-40aa-aaf1-172cb39f0711
- SPL ID
- 6164ed7f-5c4f-4ad1-b445-a3556655e4ae
- Version
- 2
- Effective date
- 2026-01-08
- Source export date
- 2026-10-12
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:29:11
| 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 Bladder 7006 | openfda.brand_name | |
| generic name | RET BLADDER | openfda.generic_name | |
| manufacturer name | Professional Complementary Health Formulas | openfda.manufacturer_name | |
| ndc | package | 63083-7006-1 | openfda.package_ndc |
| ndc | product | 63083-7006 | openfda.product_ndc |
| ndc11 | package | 63083700601 | derived:openfda.package_ndc |
| spl id | 6164ed7f-5c4f-4ad1-b445-a3556655e4ae | id | |
| spl set id | f1d354e7-3d72-40aa-aaf1-172cb39f0711 | set_id | |
| unii | 2P3VWU3H10 | openfda.unii | |
| unii | 28M1820ACT | openfda.unii | |
| unii | XBP5X7E70R | openfda.unii | |
| unii | 00543AP1JV | openfda.unii | |
| unii | S13FA2GQG9 | openfda.unii | |
| unii | QDL83WN8C2 | openfda.unii | |
| unii | 07YL55QKZ9 | openfda.unii | |
| unii | 451W47IQ8X | openfda.unii | |
| unii | 1L24V9R23S | openfda.unii | |
| unii | 24K790T39B | openfda.unii | |
| unii | 1PIP394IID | openfda.unii | |
| unii | 7S82P3R43Z | openfda.unii | |
| unii | QNS6W5US1Z | openfda.unii | |
| unii | ZL25KMM82T | 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.