warnings
Warning 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.
AIM CAVITY PROTECTION Multi Benefit
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
- AIM CAVITY PROTECTION Multi Benefit
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Church & Dwight Co., Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 1d0f8a33-0b01-40e2-e054-00144ff88e88
- SPL ID
- 55802d59-ce90-478b-e063-6294a90a14e4
- Version
- 9
- Effective date
- 2026-06-01
- Source export date
- 2026-10-30
- 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/2026-10-30/7f38ccf216257b076837276c278194f298b4ccda641215a8f83814b33a860b51/drug-label-0014-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 20:01:09
| 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 | M021 | openfda.application_number | |
| brand name | AIM CAVITY PROTECTION Multi Benefit | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Church & Dwight Co., Inc. | openfda.manufacturer_name | |
| ndc | package | 10237-633-66 | openfda.package_ndc |
| ndc | package | 10237-633-45 | openfda.package_ndc |
| ndc | package | 10237-633-55 | openfda.package_ndc |
| ndc | package | 10237-633-72 | openfda.package_ndc |
| ndc | package | 10237-633-22 | openfda.package_ndc |
| ndc | package | 10237-633-60 | openfda.package_ndc |
| ndc | product | 10237-633 | openfda.product_ndc |
| ndc11 | package | 10237063360 | derived:openfda.package_ndc |
| ndc11 | package | 10237063322 | derived:openfda.package_ndc |
| ndc11 | package | 10237063345 | derived:openfda.package_ndc |
| ndc11 | package | 10237063366 | derived:openfda.package_ndc |
| ndc11 | package | 10237063372 | derived:openfda.package_ndc |
| ndc11 | package | 10237063355 | derived:openfda.package_ndc |
| rxcui | 416783 | openfda.rxcui | |
| spl id | 55802d59-ce90-478b-e063-6294a90a14e4 | id | |
| spl set id | 1d0f8a33-0b01-40e2-e054-00144ff88e88 | 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.