NDC 44946-1032 - Sodium Fluoride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 44946-1032
- Package NDCs from labels
- 44946-1032-8
- Manufacturer
- Sancilio & Company Inc
- Effective date
- 2018-03-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Sodium Fluoride - Sancilio & Company Inc | Sancilio & Company Inc | 2018-03-06 | DIETARY SUPPLEMENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 44946-1032-8 | Sodium Fluoride | 50 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 50 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 44946-1032 | SODIUM FLUORIDE SOLUTION/ DROPS [SANCILIO & COMPANY INC] | 5 | 1 package rows | 20180324_01013faa-33e3-48a4-b710-d996fac43b61.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 44946-1032-8 | ML - Milliliter | 44946-1032 | 3caf5222-8075-4f8b-929e-be5157faad63 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Sodium Fluoride | ACTIVE INGREDIENT | 8ZYQ1474W7 | SODIUM FLUORIDE SOLUTION/ DROPS [SANCILIO & COMPANY INC] | 2 | |
| Fluoride Ion | ACTIVE MOIETY | Q80VPU408O | SODIUM FLUORIDE SOLUTION/ DROPS [SANCILIO & COMPANY INC] | 2 | |
| Glycerin | INACTIVE INGREDIENT | PDC6A3C0OX | SODIUM FLUORIDE SOLUTION/ DROPS [SANCILIO & COMPANY INC] | 2 | |
| Methylparaben | INACTIVE INGREDIENT | A2I8C7HI9T | SODIUM FLUORIDE SOLUTION/ DROPS [SANCILIO & COMPANY INC] | 2 | |
| Propylene glycol | INACTIVE INGREDIENT | 6DC9Q167V3 | SODIUM FLUORIDE SOLUTION/ DROPS [SANCILIO & COMPANY INC] | 2 | |
| Propylparaben | INACTIVE INGREDIENT | Z8IX2SC1OH | SODIUM FLUORIDE SOLUTION/ DROPS [SANCILIO & COMPANY INC] | 2 | |
| Sucralose | INACTIVE INGREDIENT | 96K6UQ3ZD4 | SODIUM FLUORIDE SOLUTION/ DROPS [SANCILIO & COMPANY INC] | 2 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | SODIUM FLUORIDE SOLUTION/ DROPS [SANCILIO & COMPANY INC] | 2 | |
| Xylitol | INACTIVE INGREDIENT | VCQ006KQ1E | SODIUM FLUORIDE SOLUTION/ DROPS [SANCILIO & COMPANY INC] | 2 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Anticavity | SODIUM FLUORIDE | Walmart Inc. | af5b93e7-5cce-4e01-8df2-54494d8b2910 | 2026-02-27 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Anticavity | SODIUM FLUORIDE | Walmart Inc. | 4590ca97-130c-46b2-9ba0-38f4703ef30a | 2026-02-27 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Dermatool Hemorrhoidal | GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HCL | Papalo Group LLC | 4bc06f41-7733-ebd0-e063-6294a90af7a8 | 2026-02-26 | Warnings | PDC6A3C0OX |
| Anticavity Rinse | SODIUM FLUORIDE | Family Dollar Stores, Inc | 32a92add-c9db-4733-8e35-613825fdf081 | 2026-02-24 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Anticavity Fluoride Rinse | SODIUM FLUORIDE | Family Dollar Stores, Inc | 32ebc633-5338-4d5a-b075-f10b24761248 | 2026-02-24 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Anticavity Rinse | SODIUM FLUORIDE | H E B | 51ddc81b-1c90-4998-b538-6761ac113437 | 2026-02-24 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Anticavity | SODIUM FLUORIDE | Meijer, Inc. | 9a0b6301-2443-41f7-adeb-87578a65c26d | 2026-02-24 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Anticavity | SODIUM FLUORIDE | CVS Pharmacy, Inc. | 344c9d00-ad82-46a9-83e9-68197e1a68bb | 2026-02-23 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| TheraBreath Complete Oral Rinse | ANTICAVITY ORAL RINSE | Church & Dwight Co., Inc. | 27c33ae1-52c7-baad-e063-6394a90a0611 | 2026-02-23 | Warnings | 8ZYQ1474W7 |
| Anticavity Rinse | SODIUM FLUORIDE | Meijer, Inc. | 001777fb-196c-499a-94c8-6cdcef0958e9 | 2026-02-19 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Anticavity | SODIUM FLUORIDE | Meijer, Inc. | c628d02f-c834-42b3-b38d-6b9cdcdd0961 | 2026-02-19 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Anticavity Rinse | SODIUM FLUORIDE | Meijer, Inc. | b17f7a5d-272e-446d-803b-46a6d8e5f18f | 2026-02-19 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Anticavity Fluoride Rinse | SODIUM FLUORIDE | Meijer, Inc. | d85ce60c-ebff-461f-827a-10fddb9c2bf3 | 2026-02-19 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Alcohol-Free Anticavity | SODIUM FLUORIDE | Meijer, Inc. | c4dcb1d8-f2af-4363-8fcd-c7d1197d66ea | 2026-02-19 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Oral Antivavity | SODIUM FLUORIDE | Meijer, Inc. | af34f83f-1328-4897-9d04-72ca5a4101bf | 2026-02-19 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Anticavity | SODIUM FLUORIDE | Meijer, Inc. | acff939e-e98c-4d89-a0c4-0254dc74e672 | 2026-02-19 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Anticavity fluoride rinse | SODIUM FLUORIDE | Meijer, Inc. | 0bb9fb5f-1893-4187-b60b-05319a8fac6a | 2026-02-19 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Listerine Total Care Intense Anticavity Fluoride Mouthwash | SODIUM FLUORIDE | Kenvue Brands LLC | 4b0404af-309f-7c31-e063-6294a90a5aa1 | 2026-02-18 | Warnings | 8ZYQ1474W7 |
| Anticavity | SODIUM FLUORIDE | Target Corporation | abfc1973-60ab-44e5-8147-33739d8bd7a3 | 2026-02-18 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Anticavity Fluoride Rinse | SODIUM FLUORIDE | Target Corporation | 3e4119b2-9506-4305-8cff-163f700265d0 | 2026-02-18 | Warnings, Adverse reactions | 8ZYQ1474W7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.