Up and Up Sensitive Toothpaste Whitening
- Product NDC
- 67659-079
- 11-digit product format
- 676590079
- Labeler code
- 67659
- Product ID
- 67659-079_18708150-8558-400f-84b2-62ea4a8ddc0e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Potassium Nitrate and Sodium Fluoride
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- Team Technologies, Inc
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-08-25
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 5 mg/g; 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 |
|---|
| 67659-079-01 | Up and Up Sensitive Toothpaste Whitening | 113 g in 1 TUBE | PASTE | 113 | | 1 |
| 67659-079-02 | Up and Up Sensitive Toothpaste Whitening | 1 in 1 CARTON | PASTE | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67659-079 | UP AND UP SENSITIVE TOOTHPASTE WHITENING (POTASSIUM NITRATE AND SODIUM FLUORIDE) PASTE [TEAM TECHNOLOGIES, INC] | 1 | Legacy NDC, 2 package rows | 20100831_3de46220-5e45-4d10-9ebd-6d105e9c3a13.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 67659-079-01 | 67659007901 | 113 g in 1 TUBE | 113 g | Historical |
| 67659-079-02 | 67659007902 | 1 in 1 CARTON | | Historical |