ARC
- Product NDC
- 69423-889
- 11-digit product format
- 694230889
- Labeler code
- 69423
- Product ID
- 69423-889_dda4adab-bbd6-d99a-e053-2995a90a227b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Procter & Gamble Manufacturing Company
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-01-05
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 1 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69423-889 | ARC WHITENING (SODIUM FLUORIDE) PASTE, DENTIFRICE [PROCTER & GAMBLE MANUFACTURING COMPANY] | 4 | Legacy NDC | 20250110_dda499e4-98d2-4407-e053-2995a90ae74b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69423-889-40 | 69423088940 | 1 TUBE in 1 CARTON (69423-889-40) > 113 g in 1 TUBE | 1 tube | 2021-01-05 | 0000-00-00 | No | No | Current |