warnings and cautions
Warnings Contens under pressure. Do not puncture or incinerate. Keep out of reach of children. Store between 50-80F. Keep from freezing. do not spray toward open flame.
Acclean Foam Fluoride 60 Second Application
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 Foam Fluoride 60 Second Application
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Henry Schein
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- c10af938-0537-2425-e053-2a95a90ad608
- SPL ID
- 06d4de64-6d8f-6bfb-e063-6294a90a40eb
- Version
- 3
- Effective date
- 2023-10-03
- Source export date
- 2026-10-27
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:46:42
| 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 |
|---|---|---|---|
| brand name | Acclean Foam Fluoride 60 Second Application | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Henry Schein | openfda.manufacturer_name | |
| ndc | package | 0404-1701-44 | openfda.package_ndc |
| ndc | package | 0404-1721-44 | openfda.package_ndc |
| ndc | package | 0404-1711-44 | openfda.package_ndc |
| ndc | package | 0404-1741-44 | openfda.package_ndc |
| ndc | package | 0404-1731-44 | openfda.package_ndc |
| ndc | product | 0404-1741 | openfda.product_ndc |
| ndc | product | 0404-1731 | openfda.product_ndc |
| ndc | product | 0404-1721 | openfda.product_ndc |
| ndc | product | 0404-1701 | openfda.product_ndc |
| ndc | product | 0404-1711 | openfda.product_ndc |
| ndc11 | package | 00404174144 | derived:openfda.package_ndc |
| ndc11 | package | 00404170144 | derived:openfda.package_ndc |
| ndc11 | package | 00404172144 | derived:openfda.package_ndc |
| ndc11 | package | 00404171144 | derived:openfda.package_ndc |
| ndc11 | package | 00404173144 | derived:openfda.package_ndc |
| rxcui | 248389 | openfda.rxcui | |
| spl id | 06d4de64-6d8f-6bfb-e063-6294a90a40eb | id | |
| spl set id | c10af938-0537-2425-e053-2a95a90ad608 | 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.