Product NDC: | 68400-111 |
Proprietary Name: | Gelato APF Gel Strawberry 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: | 68400-111 |
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: | 68400-111-15 |
Package Description: | 454 g in 1 BOTTLE, PLASTIC (68400-111-15) |
NDC Code | 68400-111-15 |
Proprietary Name | Gelato APF Gel Strawberry 16oz |
Package Description | 454 g in 1 BOTTLE, PLASTIC (68400-111-15) |
Product NDC | 68400-111 |
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 |