Product NDC: | 64778-0396 |
Proprietary Name: | Denti-Care Denti-Freeze |
Non Proprietary Name: | benzocaine, tetracaine hydrochloride |
Active Ingredient(s): | .18; .02 g/g; g/g & nbsp; benzocaine, tetracaine hydrochloride |
Administration Route(s): | DENTAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64778-0396 |
Labeler Name: | AR Medicom Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20000201 |
Package NDC: | 64778-0396-1 |
Package Description: | 28.4 g in 1 JAR (64778-0396-1) |
NDC Code | 64778-0396-1 |
Proprietary Name | Denti-Care Denti-Freeze |
Package Description | 28.4 g in 1 JAR (64778-0396-1) |
Product NDC | 64778-0396 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | benzocaine, tetracaine hydrochloride |
Dosage Form Name | GEL |
Route Name | DENTAL |
Start Marketing Date | 20000201 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | AR Medicom Inc |
Substance Name | BENZOCAINE; TETRACAINE HYDROCHLORIDE |
Strength Number | .18; .02 |
Strength Unit | g/g; g/g |
Pharmaceutical Classes | Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Ester Local Anesthetic [EPC],Esters [Chemical/Ingredient],Local Anesthesia [PE] |