| Product NDC: | 37205-607 |
| Proprietary Name: | Leader Oral Pain Relief |
| Non Proprietary Name: | Benzocaine 20% |
| Active Ingredient(s): | 200 mg/g & nbsp; Benzocaine 20% |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37205-607 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120808 |
| Package NDC: | 37205-607-06 |
| Package Description: | 1 TUBE in 1 CARTON (37205-607-06) > 14.2 g in 1 TUBE (37205-607-05) |
| NDC Code | 37205-607-06 |
| Proprietary Name | Leader Oral Pain Relief |
| Package Description | 1 TUBE in 1 CARTON (37205-607-06) > 14.2 g in 1 TUBE (37205-607-05) |
| Product NDC | 37205-607 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine 20% |
| Dosage Form Name | GEL |
| Route Name | ORAL |
| Start Marketing Date | 20120808 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Cardinal Health |
| Substance Name | BENZOCAINE |
| Strength Number | 200 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |