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DT Whitening Anticavity Fluoride
DT Whitening Anticavity Fluoride - 50523-740-64 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of DT Whitening Anticavity Fluoride
| Product NDC: | 50523-740 |
| Proprietary Name: | DT Whitening Anticavity Fluoride |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | .76 g/100g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DT Whitening Anticavity Fluoride
| Product NDC: | 50523-740 |
| Labeler Name: | Volume Distributors, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110722 |
Package Information of DT Whitening Anticavity Fluoride
| Package NDC: | 50523-740-64 |
| Package Description: | 1 TUBE in 1 BOX (50523-740-64) > 181 g in 1 TUBE |
NDC Information of DT Whitening Anticavity Fluoride
| NDC Code | 50523-740-64 |
| Proprietary Name | DT Whitening Anticavity Fluoride |
| Package Description | 1 TUBE in 1 BOX (50523-740-64) > 181 g in 1 TUBE |
| Product NDC | 50523-740 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20110722 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Volume Distributors, Inc. |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | .76 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
