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OraBrite
OraBrite - 54371-471-03 - (SODIUM FLUORIDE)
Drug Information of OraBrite
| Product NDC: | 54371-471 |
| Proprietary Name: | OraBrite |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | .22 g/100g & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OraBrite
| Product NDC: | 54371-471 |
| Labeler Name: | Oraline, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111031 |
Package Information of OraBrite
| Package NDC: | 54371-471-03 |
| Package Description: | 78 g in 1 TUBE (54371-471-03) |
NDC Information of OraBrite
| NDC Code | 54371-471-03 |
| Proprietary Name | OraBrite |
| Package Description | 78 g in 1 TUBE (54371-471-03) |
| Product NDC | 54371-471 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20111031 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Oraline, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .22 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
