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LEVEL WINTERMINT FIVE WHITENING FORMULA ANTICAVITY
LEVEL WINTERMINT FIVE WHITENING FORMULA ANTICAVITY - 50001-121-50 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of LEVEL WINTERMINT FIVE WHITENING FORMULA ANTICAVITY
| Product NDC: | 50001-121 |
| Proprietary Name: | LEVEL WINTERMINT FIVE WHITENING FORMULA ANTICAVITY |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | .76 g/100g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEVEL WINTERMINT FIVE WHITENING FORMULA ANTICAVITY
| Product NDC: | 50001-121 |
| Labeler Name: | LEVEL ORAL CARE, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100816 |
Package Information of LEVEL WINTERMINT FIVE WHITENING FORMULA ANTICAVITY
| Package NDC: | 50001-121-50 |
| Package Description: | 141.7 g in 1 TUBE (50001-121-50) |
NDC Information of LEVEL WINTERMINT FIVE WHITENING FORMULA ANTICAVITY
| NDC Code | 50001-121-50 |
| Proprietary Name | LEVEL WINTERMINT FIVE WHITENING FORMULA ANTICAVITY |
| Package Description | 141.7 g in 1 TUBE (50001-121-50) |
| Product NDC | 50001-121 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20100816 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | LEVEL ORAL CARE, LLC |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | .76 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
