Home
>
National Drug Code (NDC)
>
Denti-Care Denti-Freeze
Denti-Care Denti-Freeze - 64778-0399-1 - (benzocaine, tetracaine hydrochloride)
Drug Information of Denti-Care Denti-Freeze
| Product NDC: | 64778-0399 |
| 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) |
Labeler Information of Denti-Care Denti-Freeze
| Product NDC: | 64778-0399 |
| Labeler Name: | AR Medicom Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20000201 |
Package Information of Denti-Care Denti-Freeze
| Package NDC: | 64778-0399-1 |
| Package Description: | 28.4 g in 1 JAR (64778-0399-1) |
NDC Information of Denti-Care Denti-Freeze
| NDC Code | 64778-0399-1 |
| Proprietary Name | Denti-Care Denti-Freeze |
| Package Description | 28.4 g in 1 JAR (64778-0399-1) |
| Product NDC | 64778-0399 |
| 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] |
