SKYLINE HERBALS
- Product NDC
- 80239-9138
- 11-digit product format
- 802399138
- Labeler code
- 80239
- Product ID
- 80239-9138_ae30c235-46b0-65a3-e053-2995a90a7adf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Monofluorophosphate
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- SKYLINE HERBALS PRIVATE LIMITED
- Application
- part355
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2019-07-23
- Marketing end
- 0000-00-00
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- 8 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 80239-9138-6 | SKYLINE HERBALS | 43 g in 1 TUBE | PASTE, DENTIFRICE | 43 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80239-9138 | SKYLINE HERBALS (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [SKYLINE HERBALS PRIVATE LIMITED] | 1 | Legacy NDC, 1 package rows | 20200901_ae30bf18-8b14-1519-e053-2a95a90a5628.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 |
|---|
| 80239-9138-6 | 80239913806 | 43 g in 1 TUBE (80239-9138-6) | 43 g | 2019-07-23 | 0000-00-00 | No | No | Current |