Acclean Anti-Cavity
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
- Acclean Anti-Cavity
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Henry Schein, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 7db9f10e-8f7b-41b2-a158-21e69e8256eb
- SPL ID
- fd35a40b-539d-4a27-a7f2-e360cc07d71b
- Version
- 1
- Effective date
- 2024-11-14
- Source export date
- 2026-09-28
- 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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:45:30
| 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 |
|---|---|---|---|
| brand name | Acclean Anti-Cavity | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Henry Schein, Inc. | openfda.manufacturer_name | |
| ndc | package | 0404-0173-04 | openfda.package_ndc |
| ndc | product | 0404-0173 | openfda.product_ndc |
| ndc11 | package | 00404017304 | derived:openfda.package_ndc |
| rxcui | 392038 | openfda.rxcui | |
| spl id | fd35a40b-539d-4a27-a7f2-e360cc07d71b | id | |
| spl set id | 7db9f10e-8f7b-41b2-a158-21e69e8256eb | set_id | |
| unii | 8ZYQ1474W7 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
5 WARNINGS AND PRECAUTIONS DO NOT SWALLOW. Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away. Prolonged daily ingestion may result in various degrees of dental fluorosis in children with developing dentition, especially if the water fluoridation exceeds 0.6 ppm, since younger children frequently cannot perform the brushing process without significant swallowing. Use in children under age 6 years requires special supervision to prevent repeated swallowing of toothpaste which could cause dental fluorosis. Read directions carefully before using. Keep out of reach of infants and children. Sensitive teeth may indicate a serious problem that may need prompt care by a dentist. See your dentist if the problem persists or worsens. Do not use this product longer than 4 weeks unless recommended by a dentist or physician.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
6 ADVERSE REACTIONS Allergic reactions and other idiosyncrasies have rarely been reported.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.