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NEUTRA MAXX 5000
NEUTRA MAXX 5000 - 63783-504-06 - (SODIUM FLUORIDE)
Drug Information of NEUTRA MAXX 5000
| Product NDC: | 63783-504 |
| Proprietary Name: | NEUTRA MAXX 5000 |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | 1.428 g/120g & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NEUTRA MAXX 5000
| Product NDC: | 63783-504 |
| Labeler Name: | Massco Dental A Division of Dunagin Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19890101 |
Package Information of NEUTRA MAXX 5000
| Package NDC: | 63783-504-06 |
| Package Description: | 120 g in 1 BOTTLE, DISPENSING (63783-504-06) |
NDC Information of NEUTRA MAXX 5000
| NDC Code | 63783-504-06 |
| Proprietary Name | NEUTRA MAXX 5000 |
| Package Description | 120 g in 1 BOTTLE, DISPENSING (63783-504-06) |
| Product NDC | 63783-504 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | GEL |
| Route Name | ORAL |
| Start Marketing Date | 19890101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Massco Dental A Division of Dunagin Pharmaceuticals |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 1.428 |
| Strength Unit | g/120g |
| Pharmaceutical Classes |
