ARC
- Product NDC
- 69423-888
- 11-digit product format
- 694230888
- Labeler code
- 69423
- Product ID
- 69423-888_dae32c29-cf6a-1eb4-e053-2995a90a787a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- RINSE
- Route
- ORAL
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-06-01
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 0 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 8ZYQ1474W7 | SODIUM FLUORIDE | 7681-49-4 | SODIUM FLUORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69423-888-16 | 69423088816 | 475 mL in 1 BOTTLE, PLASTIC (69423-888-16) | 475 ml | 2021-06-01 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ARC After Whitening Rinse | The Procter & Gamble Manufacturing Company | 2025-07-31 | HUMAN OTC DRUG LABEL | 7 |