Mini Duo
- Product NDC
- 72164-102
- 11-digit product format
- 721640102
- Labeler code
- 72164
- Product ID
- 72164-102_ebe7da86-6acd-c9d4-e053-2a95a90a8ff9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- POTASSIUM NITRATE, SODIUM FLUORIDE
- Dosage form
- KIT
- Labeler
- Smiletwice, Inc.
- Application
- part355B
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-03-01
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 72164-000-02 | Mini Duo | 23 g in 1 TUBE | PASTE | 23 g | 50 mg in 1g | 3 |
| 72164-001-02 | Mini Duo | 23 g in 1 TUBE | PASTE | 23 g | 50 mg in 1g | 3 |
| 72164-102-23 | Mini Duo | 1 in 1 KIT | KIT | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72164-102 | MINI DUO (POTASSIUM NITRATE, SODIUM FLUORIDE) KIT [SMILETWICE, INC.] | 3 | Legacy NDC, 3 package rows | 20231221_99509d36-cae4-43a7-9ae7-74c101b1bee9.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 |
|---|
| 72164-000-02 | 72164000002 | 23 g in 1 TUBE | 23 g | | | | | Historical |
| 72164-001-02 | 72164000102 | 23 g in 1 TUBE | 23 g | | | | | Historical |
| 72164-102-23 | 72164010223 | 1 KIT in 1 KIT (72164-102-23) * 23 g in 1 TUBE (72164-001-02) * 23 g in 1 TUBE (72164-000-02) | 1 kit | 2020-03-01 | 0000-00-00 | No | No | Current |