Up and Up Anticavity Toothpaste Whitening
- Product NDC
- 67659-082
- 11-digit product format
- 676590082
- Labeler code
- 67659
- Product ID
- 67659-082_a4b74051-aca6-4926-a464-41bf4539d968
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Team Technologies, Inc
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-08-25
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE
- Active strength
- 2 mg/g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67659-082-01 | Up and Up Anticavity Toothpaste Whitening | 181.4 g in 1 TUBE | PASTE, DENTIFRICE | 181.4 | | 1 |
| 67659-082-02 | Up and Up Anticavity Toothpaste Whitening | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67659-082 | UP AND UP ANTICAVITY TOOTHPASTE WHITENING (SODIUM FLUORIDE) PASTE, DENTIFRICE [TEAM TECHNOLOGIES, INC] | 1 | Legacy NDC, 2 package rows | 20100831_1cb8693e-5601-441e-b228-71de1c6d6906.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 67659-082-01 | 67659008201 | 181.4 g in 1 TUBE | 181.4 g | Historical |
| 67659-082-02 | 67659008202 | 1 in 1 CARTON | | Historical |