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NBF Gingival
NBF Gingival - 23636-1001-1 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of NBF Gingival
| Product NDC: | 23636-1001 |
| Proprietary Name: | NBF Gingival |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | .4 g/30g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NBF Gingival
| Product NDC: | 23636-1001 |
| Labeler Name: | NanoCureTech |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20111111 |
Package Information of NBF Gingival
| Package NDC: | 23636-1001-1 |
| Package Description: | 30 g in 1 TUBE (23636-1001-1) |
NDC Information of NBF Gingival
| NDC Code | 23636-1001-1 |
| Proprietary Name | NBF Gingival |
| Package Description | 30 g in 1 TUBE (23636-1001-1) |
| Product NDC | 23636-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | GEL |
| Route Name | DENTAL |
| Start Marketing Date | 20111111 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | NanoCureTech |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | .4 |
| Strength Unit | g/30g |
| Pharmaceutical Classes |
