| Product NDC: | 68400-108 |
| Proprietary Name: | Gelato APF Gel Mint 16oz |
| Non Proprietary Name: | APF Gel |
| Active Ingredient(s): | 9.5 g/454g & nbsp; APF Gel |
| Administration Route(s): | DENTAL; ORAL; TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68400-108 |
| Labeler Name: | Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20121214 |
| Package NDC: | 68400-108-15 |
| Package Description: | 454 g in 1 BOTTLE, PLASTIC (68400-108-15) |
| NDC Code | 68400-108-15 |
| Proprietary Name | Gelato APF Gel Mint 16oz |
| Package Description | 454 g in 1 BOTTLE, PLASTIC (68400-108-15) |
| Product NDC | 68400-108 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | APF Gel |
| Dosage Form Name | GEL |
| Route Name | DENTAL; ORAL; TOPICAL |
| Start Marketing Date | 20121214 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 9.5 |
| Strength Unit | g/454g |
| Pharmaceutical Classes |