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.
Fluorite 8118
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
- Fluorite 8118
- Generic name
- FLUORITE
- Manufacturer
- Professional Complementary Health Formulas
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 27d3a249-494b-4783-9e08-808296c7b2d2
- SPL ID
- 683cd94d-7bf4-4ba4-b90b-8df1fda07995
- Version
- 2
- Effective date
- 2026-01-08
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:38:48
| 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 | Fluorite 8118 | openfda.brand_name | |
| generic name | FLUORITE | openfda.generic_name | |
| manufacturer name | Professional Complementary Health Formulas | openfda.manufacturer_name | |
| ndc | package | 63083-8118-2 | openfda.package_ndc |
| ndc | product | 63083-8118 | openfda.product_ndc |
| ndc11 | package | 63083811802 | derived:openfda.package_ndc |
| spl id | 683cd94d-7bf4-4ba4-b90b-8df1fda07995 | id | |
| spl set id | 27d3a249-494b-4783-9e08-808296c7b2d2 | set_id | |
| unii | O3B55K4YKI | 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.