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
- Family Dollar Stores, Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 32ebc633-5338-4d5a-b075-f10b24761248
- SPL ID
- 4b933738-3759-6543-e063-6294a90a67d2
- Version
- 15
- Effective date
- 2026-02-24
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:27:08
| 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 | Family Dollar Stores, Inc | openfda.manufacturer_name | |
| ndc | package | 55319-163-86 | openfda.package_ndc |
| ndc | product | 55319-163 | openfda.product_ndc |
| ndc11 | package | 55319016386 | derived:openfda.package_ndc |
| rxcui | 313029 | openfda.rxcui | |
| spl id | 4b933738-3759-6543-e063-6294a90a67d2 | id | |
| spl set id | 32ebc633-5338-4d5a-b075-f10b24761248 | set_id | |
| unii | 8ZYQ1474W7 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warning for this product
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse Reaction DISTRIBUTED BY: MIDWOOD BRANDS, LLC 500 VOLVO PKWY, CHESAPEAKE, VA 23320 USA MADE IN THE US WITH US AND FOREIGN COMPONENTS. NOT 100% SATISFIED? Return within 30 days to the store of purchase for a refund (with receipt) or Exchange. DSP-TN-21091 DSP-MO-20087
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.