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 Large Intestine 7004
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 Large Intestine 7004
- Generic name
- RET LARGE INTESTINE
- Manufacturer
- Professional Complementary Health Formulas
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f1d07d3b-be59-4021-a9cb-8cb9b5b2aff5
- SPL ID
- 0b0b8e6a-f2b9-49ca-8921-521f3fbf5624
- Version
- 2
- Effective date
- 2026-01-08
- Source export date
- 2026-10-22
- 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/2026-10-22/cecf96da1d46fddb232fa67374b5f0412041c54b0ff227afc2f842c4c7955161/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
- Import run
- 20261023T001338Z
- Imported at
- 2026-10-23 01:14:00
| 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 | RET Large Intestine 7004 | openfda.brand_name | |
| generic name | RET LARGE INTESTINE | openfda.generic_name | |
| manufacturer name | Professional Complementary Health Formulas | openfda.manufacturer_name | |
| ndc | package | 63083-7004-1 | openfda.package_ndc |
| ndc | product | 63083-7004 | openfda.product_ndc |
| ndc11 | package | 63083700401 | derived:openfda.package_ndc |
| spl id | 0b0b8e6a-f2b9-49ca-8921-521f3fbf5624 | id | |
| spl set id | f1d07d3b-be59-4021-a9cb-8cb9b5b2aff5 | set_id | |
| unii | 192426I5JU | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | 324Y4038G2 | openfda.unii | |
| unii | 311PNK9CDZ | openfda.unii | |
| unii | 95IT3W8JZE | openfda.unii | |
| unii | HW54500A89 | openfda.unii | |
| unii | 1L24V9R23S | openfda.unii | |
| unii | 2E32821G6I | openfda.unii | |
| unii | 1K573LC5TV | openfda.unii | |
| unii | Y0F0BU8RDU | openfda.unii | |
| unii | 11B89M58UN | openfda.unii | |
| unii | C88X29Y479 | 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.