NDC 79481-0201-01 - Anticavity Rinse
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
- 79481-0201
- Requested NDC
- 79481-0201-01
- Package NDCs from labels
- 79481-0201-1, 79481-0201-01
- Manufacturer
- Meijer, Inc. | Nice-Pak Products, LLC
- Effective date
- 2026-02-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Anticavity Rinse - Meijer, Inc. | Nice-Pak Products, LLC | Meijer, Inc. | Nice-Pak Products, LLC | 2026-02-19 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-0201-1 | Anticavity Rinse | 532 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 532 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79481-0201 | ANTICAVITY RINSE (SODIUM FLUORIDE) MOUTHWASH [MEIJER DISTRIBUTION, INC.] | 7 | Current NDC, Legacy NDC, 1 package rows | 20240820_b17f7a5d-272e-446d-803b-46a6d8e5f18f.zip |
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.