| Product NDC: | 68400-112 |
| Proprietary Name: | Gelato Fluoride |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 1.5375 g/125g & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL; ORAL; TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68400-112 |
| Labeler Name: | Deepak Products, inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120202 |
| Package NDC: | 68400-112-12 |
| Package Description: | 125 g in 1 BOTTLE, SPRAY (68400-112-12) |
| NDC Code | 68400-112-12 |
| Proprietary Name | Gelato Fluoride |
| Package Description | 125 g in 1 BOTTLE, SPRAY (68400-112-12) |
| Product NDC | 68400-112 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | DENTAL; ORAL; TOPICAL |
| Start Marketing Date | 20120202 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Deepak Products, inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 1.5375 |
| Strength Unit | g/125g |
| Pharmaceutical Classes |