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Dentree
Dentree - 76170-101-50 - (sodium fluoride)
Drug Information of Dentree
| Product NDC: | 76170-101 |
| Proprietary Name: | Dentree |
| Non Proprietary Name: | sodium fluoride |
| Active Ingredient(s): | .22 g/1000mL & nbsp; sodium fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dentree
| Product NDC: | 76170-101 |
| Labeler Name: | e-soup Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120401 |
Package Information of Dentree
| Package NDC: | 76170-101-50 |
| Package Description: | 50 mL in 1 BOTTLE, PUMP (76170-101-50) |
NDC Information of Dentree
| NDC Code | 76170-101-50 |
| Proprietary Name | Dentree |
| Package Description | 50 mL in 1 BOTTLE, PUMP (76170-101-50) |
| Product NDC | 76170-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sodium fluoride |
| Dosage Form Name | GEL, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20120401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | e-soup Co., Ltd. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .22 |
| Strength Unit | g/1000mL |
| Pharmaceutical Classes |
