NBF Gingival
- Product NDC
- 23636-1001
- 11-digit product format
- 236361001
- Labeler code
- 23636
- Product ID
- 23636-1001_c9d5436a-b2fe-4e0f-aaa9-4a584fbd59e9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM MONOFLUOROPHOSPHATE
- Dosage form
- GEL
- Route
- DENTAL
- Labeler
- NanoCureTech
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-11-11
- Marketing end
- 0000-00-00
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- 0 g/30g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 23636-1001-1 | NBF Gingival | 30 g in 1 TUBE | GEL | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 23636-1001 | NBF GINGIVAL (SODIUM MONOFLUOROPHOSPHATE) GEL [NANOCURETECH] | 1 | Legacy NDC, 1 package rows | 20111115_028fbb3a-87f4-4f82-88e5-346f5a17753c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 23636-1001-1 | 23636100101 | 30 g in 1 TUBE | 30 g | Historical |