Product NDC: | 10216-3091 |
Proprietary Name: | Topex |
Non Proprietary Name: | Benzocaine |
Active Ingredient(s): | 220 mg/g & nbsp; Benzocaine |
Administration Route(s): | DENTAL |
Dosage Form(s): | GEL, DENTIFRICE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10216-3091 |
Labeler Name: | DENTSPLY Caulk |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19630219 |
Package NDC: | 10216-3091-1 |
Package Description: | 100 g in 1 JAR (10216-3091-1) |
NDC Code | 10216-3091-1 |
Proprietary Name | Topex |
Package Description | 100 g in 1 JAR (10216-3091-1) |
Product NDC | 10216-3091 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Benzocaine |
Dosage Form Name | GEL, DENTIFRICE |
Route Name | DENTAL |
Start Marketing Date | 19630219 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | DENTSPLY Caulk |
Substance Name | BENZOCAINE |
Strength Number | 220 |
Strength Unit | mg/g |
Pharmaceutical Classes | Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient] |