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.
AMERFRESH FLUORIDE gel
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
- AMERFRESH FLUORIDE gel
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Yangzhou ONE & ONLY Personal Care Products Co., LTD
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 86279b4d-82e5-45b5-9ba7-94fe3620b850
- SPL ID
- 2bce0b25-f314-443b-e063-6394a90a4102
- Version
- 1
- Effective date
- 2025-01-16
- Source export date
- 2026-10-12
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:56:17
| Harmonized routes |
|---|
| TOPICAL |
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 | M021 | openfda.application_number | |
| brand name | AMERFRESH FLUORIDE gel | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Yangzhou ONE & ONLY Personal Care Products Co., LTD | openfda.manufacturer_name | |
| ndc | package | 85162-001-01 | openfda.package_ndc |
| ndc | package | 85162-001-06 | openfda.package_ndc |
| ndc | package | 85162-001-02 | openfda.package_ndc |
| ndc | package | 85162-001-04 | openfda.package_ndc |
| ndc | package | 85162-001-05 | openfda.package_ndc |
| ndc | package | 85162-001-03 | openfda.package_ndc |
| ndc | package | 85162-001-07 | openfda.package_ndc |
| ndc | product | 85162-001 | openfda.product_ndc |
| ndc11 | package | 85162000106 | derived:openfda.package_ndc |
| ndc11 | package | 85162000104 | derived:openfda.package_ndc |
| ndc11 | package | 85162000102 | derived:openfda.package_ndc |
| ndc11 | package | 85162000103 | derived:openfda.package_ndc |
| ndc11 | package | 85162000105 | derived:openfda.package_ndc |
| ndc11 | package | 85162000101 | derived:openfda.package_ndc |
| ndc11 | package | 85162000107 | derived:openfda.package_ndc |
| rxcui | 245598 | openfda.rxcui | |
| spl id | 2bce0b25-f314-443b-e063-6394a90a4102 | id | |
| spl set id | 86279b4d-82e5-45b5-9ba7-94fe3620b850 | set_id | |
| unii | 8ZYQ1474W7 | 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.