Vanilla Lavender Mint
- Product NDC
- 72164-007
- 11-digit product format
- 721640007
- Labeler code
- 72164
- Product ID
- 72164-007_d15ef84e-9e77-3e3c-e053-2a95a90ac1a8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- POTASSIUM NITRATE, SODIUM FLUORIDE
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Smiletwice, Inc.
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-03-01
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 50 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 72164-007-00 | Vanilla Lavender Mint | 96 g in 1 TUBE | PASTE, DENTIFRICE | 96 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72164-007 | VANILLA LAVENDER MINT (POTASSIUM NITRATE, SODIUM FLUORIDE) PASTE, DENTIFRICE [SMILETWICE, INC.] | 2 | Legacy NDC, 1 package rows | 20231222_c42b9e55-a621-4e26-8184-9a8c58b32c02.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72164-007-00 | 72164000700 | 96 g in 1 TUBE (72164-007-00) | 96 g | 2022-03-01 | 0000-00-00 | No | No | Current |