Lucky Super Soft
- Product NDC
- 20276-554
- 11-digit product format
- 202760554
- Labeler code
- 20276
- Product ID
- 20276-554_7e18b22d-0062-c0c0-e053-2991aa0ab53c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium monofluorophosphate
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Delta Brands Inc
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-03-31
- Marketing end
- 0000-00-00
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- 8 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 20276-554-01 | Lucky Super SoftAnti Cavity | 2 in 1 BOX | PASTE, DENTIFRICE | 2 | | 4 |
| 20276-554-04 | Lucky Super SoftAnti Cavity | 113 g in 1 TUBE | PASTE, DENTIFRICE | 113 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 20276-554 | LUCKY SUPER SOFT ANTI CAVITY (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [DELTA BRANDS INC] | 4 | Legacy NDC, 2 package rows | 20181229_4d24da8e-1eb3-20ca-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 20276-554-01 | 20276055401 | 2 in 1 BOX | | Historical |
| 20276-554-04 | 20276055404 | 113 g in 1 TUBE | 113 g | Historical |