UPC 801803 00211 MegaFresh Gel Fluoride Tooth is a Dental Paste, Dentifrice in the Human Otc Drug category. It is labeled and distributed by American Amenities, Inc.. The primary component is Sodium Fluoride.
| Product ID | 54157-109_298788aa-35a5-48f2-acad-c2187917f047 |
| NDC | 54157-109 |
| Product Type | Human Otc Drug |
| Proprietary Name | UPC 801803 00211 MegaFresh Gel Fluoride Tooth |
| Generic Name | Sodium Fluoride |
| Dosage Form | Paste, Dentifrice |
| Route of Administration | DENTAL |
| Marketing Start Date | 2017-06-03 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part355 |
| Labeler Name | American Amenities, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Active Ingredient Strength | 0 g/100g |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2017-06-03 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-03 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-03 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-03 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-03 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-03 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-03 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-03 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-03 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | OTC monograph final |
| Application Number | part355 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2017-06-03 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| SODIUM FLUORIDE | .1 g/100g |
| SPL SET ID: | 42824602-9b12-449d-9888-ade5a97ce129 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 54157-109 | UPC 801803 00211 MegaFresh Gel Fluoride Tooth | UPC 801803 00211 MegaFresh Gel Fluoride Tooth |
| 0135-0234 | AQUAFRESH | sodium fluoride |
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