warnings
Warning for this product
Anticavity Fluoride Rinse
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
- Anticavity Fluoride Rinse
- Generic name
- SODIUM FLUORIDE
- Manufacturer
- Target Corporation
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3e4119b2-9506-4305-8cff-163f700265d0
- SPL ID
- 4b1e3881-571e-9711-e063-6294a90a2f94
- Version
- 19
- Effective date
- 2026-02-18
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:11:44
| Harmonized routes |
|---|
| ORAL |
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 | Anticavity Fluoride Rinse | openfda.brand_name | |
| generic name | SODIUM FLUORIDE | openfda.generic_name | |
| manufacturer name | Target Corporation | openfda.manufacturer_name | |
| ndc | package | 11673-163-86 | openfda.package_ndc |
| ndc | product | 11673-163 | openfda.product_ndc |
| ndc11 | package | 11673016386 | derived:openfda.package_ndc |
| rxcui | 313029 | openfda.rxcui | |
| spl id | 4b1e3881-571e-9711-e063-6294a90a2f94 | id | |
| spl set id | 3e4119b2-9506-4305-8cff-163f700265d0 | set_id | |
| unii | 8ZYQ1474W7 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse reaction Distributed by Target Corporation Minneapolis, MN 55403 Made in the U.S. with U.S. and foreign components. TM & ©2024 Target Brands, Inc. DSP-TN-21091 DSP-MO-20087
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.