warnings
Warnings Keep out of the reach of children under 6 years of age. If more than used for brushing is accidently swallowed, get medical help or contact a Poison Control Center immediately. Keep out of reach of children.
Charm Tex FLUORIDE
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
- Charm Tex FLUORIDE
- Generic name
- SODIUM MONOFLUOROPHOSPHATE
- Manufacturer
- Jiangsu Gold Worldworks Household Chemicals Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2bddc69a-0c0f-47fc-bc98-90c2ec70dd6f
- SPL ID
- 53169607-6939-663b-e063-6394a90a082b
- Version
- 1
- Effective date
- 2026-05-31
- Source export date
- 2026-10-12
- Source partition
- 14
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:12:19
| Harmonized routes |
|---|
| DENTAL |
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 |
|---|---|---|---|
| application number | M017 | openfda.application_number | |
| brand name | Charm Tex FLUORIDE | openfda.brand_name | |
| generic name | SODIUM MONOFLUOROPHOSPHATE | openfda.generic_name | |
| manufacturer name | Jiangsu Gold Worldworks Household Chemicals Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 42086-051-03 | openfda.package_ndc |
| ndc | package | 42086-051-02 | openfda.package_ndc |
| ndc | package | 42086-051-04 | openfda.package_ndc |
| ndc | package | 42086-051-06 | openfda.package_ndc |
| ndc | package | 42086-051-05 | openfda.package_ndc |
| ndc | package | 42086-051-01 | openfda.package_ndc |
| ndc | product | 42086-051 | openfda.product_ndc |
| ndc11 | package | 42086005106 | derived:openfda.package_ndc |
| ndc11 | package | 42086005105 | derived:openfda.package_ndc |
| ndc11 | package | 42086005104 | derived:openfda.package_ndc |
| ndc11 | package | 42086005103 | derived:openfda.package_ndc |
| ndc11 | package | 42086005102 | derived:openfda.package_ndc |
| ndc11 | package | 42086005101 | derived:openfda.package_ndc |
| rxcui | 545626 | openfda.rxcui | |
| spl id | 53169607-6939-663b-e063-6394a90a082b | id | |
| spl set id | 2bddc69a-0c0f-47fc-bc98-90c2ec70dd6f | set_id | |
| unii | C810JCZ56Q | 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.