teeth desensitizing and remineralizing gel is a Dental Paste in the Human Otc Drug category. It is labeled and distributed by Fuzhou Difeng Bio-tech Co., Ltd.. The primary component is Potassium Nitrate; Sodium Fluoride.
| Product ID | 49410-200_62180c5e-1369-1c60-e053-2a91aa0a3668 |
| NDC | 49410-200 |
| Product Type | Human Otc Drug |
| Proprietary Name | teeth desensitizing and remineralizing gel |
| Generic Name | Potassium Nitrate,sodium Fluoride,sodium Monofluorophosphate |
| Dosage Form | Paste |
| Route of Administration | DENTAL |
| Marketing Start Date | 2016-03-07 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part356 |
| Labeler Name | Fuzhou Difeng Bio-tech Co., Ltd. |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Active Ingredient Strength | 50 mg/g; mg/g |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2018-01-08 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-08 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-08 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-08 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-08 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-08 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-08 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-08 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph not final |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2018-01-08 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| POTASSIUM NITRATE | 50 mg/g |
| SPL SET ID: | 2d4e6542-faa9-63f2-e054-00144ff8d46c |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |