Wintergreen Peppermint
- Product NDC
- 72164-005
- 11-digit product format
- 721640005
- Labeler code
- 72164
- Product ID
- 72164-005_48c69282-189f-8bf2-e063-6394a90acf2a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- POTASSIUM NITRATE, SODIUM FLUORIDE
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Twice Twice LLC
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-03-01
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 50; 1.5 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Wintergreen Peppermint
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM NITRATE | 50 mg/g |
| SODIUM FLUORIDE | 1.5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | RU45X2JN0Z, 8ZYQ1474W7 |
| Rxcui | 1038929 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72164-005-00 | Wintergreen Peppermint | 96 g in 1 TUBE | PASTE, DENTIFRICE | 96 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72164-005 | WINTERGREEN PEPPERMINT (POTASSIUM NITRATE, SODIUM FLUORIDE) PASTE, DENTIFRICE [TWICE TWICE LLC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250221_7b7beec2-e070-4102-a2a4-68c332fc9fb3.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 |
|---|
| 72164-005-00 | 72164000500 | 96 g in 1 TUBE (72164-005-00) | 96 g | 2022-03-01 | 0000-00-00 | No | No | Current |