Lucky Super Soft
- Product NDC
- 20276-553
- 11-digit product format
- 202760553
- Labeler code
- 20276
- Product ID
- 20276-553_7e185425-019e-6d6c-e053-2a91aa0aa696
- 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 |
|---|
| 20276-553-01 | Lucky Super SoftWhitening Anti Cavity | 2 in 1 BOX | PASTE, DENTIFRICE | 2 | | 4 |
| 20276-553-04 | Lucky Super SoftWhitening Anti 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 |
|---|
| 20276-553 | LUCKY SUPER SOFT WHITENING ANTI CAVITY (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [DELTA BRANDS INC] | 4 | Legacy NDC, 2 package rows | 20181229_4d24da8e-1ea1-20ca-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 20276-553-01 | 20276055301 | 2 in 1 BOX | | Historical |
| 20276-553-04 | 20276055304 | 113 g in 1 TUBE | 113 g | Historical |