| Product NDC: | 63736-375 |
| Proprietary Name: | Americaine |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | 5.6 g/28g & nbsp; Benzocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63736-375 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090710 |
| Package NDC: | 63736-375-01 |
| Package Description: | 1 TUBE in 1 BOX (63736-375-01) > 28 g in 1 TUBE |
| NDC Code | 63736-375-01 |
| Proprietary Name | Americaine |
| Package Description | 1 TUBE in 1 BOX (63736-375-01) > 28 g in 1 TUBE |
| Product NDC | 63736-375 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20090710 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | BENZOCAINE |
| Strength Number | 5.6 |
| Strength Unit | g/28g |
| Pharmaceutical Classes |