| Product NDC: | 53045-125 |
| Proprietary Name: | Opahl |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | 12 g/60g & nbsp; Benzocaine |
| Administration Route(s): | DENTAL; ORAL; TOPICAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 53045-125 |
| Labeler Name: | Dharma Research, inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130101 |
| Package NDC: | 53045-125-60 |
| Package Description: | 60 g in 1 BOTTLE (53045-125-60) |
| NDC Code | 53045-125-60 |
| Proprietary Name | Opahl |
| Package Description | 60 g in 1 BOTTLE (53045-125-60) |
| Product NDC | 53045-125 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Benzocaine |
| Dosage Form Name | SPRAY, METERED |
| Route Name | DENTAL; ORAL; TOPICAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Dharma Research, inc. |
| Substance Name | BENZOCAINE |
| Strength Number | 12 |
| Strength Unit | g/60g |
| Pharmaceutical Classes | Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient] |