Advanced Whitening Anticavity Fluoride
- Product NDC
- 29500-9223
- 11-digit product format
- 295009223
- Labeler code
- 29500
- Product ID
- 29500-9223_899b6434-3f80-4f56-bf3d-147230a6d0b3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM MONOFLUOROPHOSPHATE
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Personal Care Products, LLC
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-07-24
- Marketing end
- 0000-00-00
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- 1000 mg/181g
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 29500-9223-6 | Advanced Whitening Anticavity Fluoride | 181 g in 1 TUBE | PASTE, DENTIFRICE | 181 | | 1 |
| 29500-9223-6 | Advanced Whitening Anticavity Fluoride | 1 in 1 BOX | PASTE, DENTIFRICE | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 29500-9223 | ADVANCED WHITENING ANTICAVITY FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [PERSONAL CARE PRODUCTS, LLC] | 1 | Legacy NDC, 2 package rows | 20170801_62f9fb4a-d6bf-4050-999b-e198207eae7d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 29500-9223-6 | 29500922306 | 181 g in 1 TUBE | 181 g | Historical |