| Product NDC: | 64778-0498 |
| Proprietary Name: | Denti-Care Denti-Freeze |
| Non Proprietary Name: | benzocaine |
| Active Ingredient(s): | .2 g/mL & nbsp; benzocaine |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64778-0498 |
| Labeler Name: | AR Medicom Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20050728 |
| Package NDC: | 64778-0498-1 |
| Package Description: | 29.6 mL in 1 JAR (64778-0498-1) |
| NDC Code | 64778-0498-1 |
| Proprietary Name | Denti-Care Denti-Freeze |
| Package Description | 29.6 mL in 1 JAR (64778-0498-1) |
| Product NDC | 64778-0498 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benzocaine |
| Dosage Form Name | OINTMENT |
| Route Name | DENTAL |
| Start Marketing Date | 20050728 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | AR Medicom Inc |
| Substance Name | BENZOCAINE |
| Strength Number | .2 |
| Strength Unit | g/mL |
| Pharmaceutical Classes | Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient] |