ADVANCED WHITENING ANTI CAVITY FLUORIDE
- Product NDC
- 52000-035
- 11-digit product format
- 520000035
- Labeler code
- 52000
- Product ID
- 52000-035_527c64a8-4a3b-3ebd-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- PASTE
- Route
- ORAL
- Labeler
- Universal Distribution Center LLC
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-06-21
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 2 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52000-035-46 | ADVANCED WHITENING ANTI CAVITY FLUORIDE | 181 g in 1 TUBE | PASTE | 181 | | 1 |
| 52000-035-46 | ADVANCED WHITENING ANTI CAVITY FLUORIDE | 1 in 1 BOX | PASTE | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52000-035 | ADVANCED WHITENING ANTI CAVITY FLUORIDE (SODIUM FLUORIDE) PASTE [UNIVERSAL DISTRIBUTION CENTER LLC] | 1 | Legacy NDC, 2 package rows | 20170621_591ac8f2-024a-4714-8a7b-eb8dc3bea528.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 52000-035-46 | 52000003546 | 181 g in 1 TUBE | 181 g | Historical |