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Benzo-Jel
Benzo-Jel - 0404-0731-01 - (Benzocaine)
Drug Information of Benzo-Jel
| Product NDC: | 0404-0731 |
| Proprietary Name: | Benzo-Jel |
| 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) |
Labeler Information of Benzo-Jel
| Product NDC: | 0404-0731 |
| Labeler Name: | Henry Schein, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19630219 |
Package Information of Benzo-Jel
| Package NDC: | 0404-0731-01 |
| Package Description: | 34 g in 1 BOTTLE (0404-0731-01) |
NDC Information of Benzo-Jel
| NDC Code | 0404-0731-01 |
| Proprietary Name | Benzo-Jel |
| Package Description | 34 g in 1 BOTTLE (0404-0731-01) |
| Product NDC | 0404-0731 |
| 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 | Henry Schein, Inc. |
| 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] |
