Colgate
- Product NDC
- 67659-350
- 11-digit product format
- 676590350
- Labeler code
- 67659
- Product ID
- 67659-350_71c08847-9679-ff89-e053-2a95a90ad9cc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride and Triclosan
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Team Technologies, Inc
- Application
- NDA020231
- Marketing category
- NDA
- Marketing start
- 2008-08-09
- Marketing end
- 0000-00-00
- Substance
- SODIUM FLUORIDE; TRICLOSAN
- Active strength
- 2 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 67659-350-06 | ColgateTotal Advance Whitening | 226 g in 1 TUBE | PASTE, DENTIFRICE | 226 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67659-350 | COLGATE TOTAL ADVANCE WHITENING (SODIUM FLUORIDE AND TRICLOSAN) PASTE, DENTIFRICE [TEAM TECHNOLOGIES, INC] | 2 | Legacy NDC, 1 package rows | 20181206_334a3704-d08f-0a85-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 67659-350-06 | 67659035006 | 226 g in 1 TUBE | 226 g | Historical |