| Product NDC: | 37205-122 |
| Proprietary Name: | LEADER ORAL ANALGESIC |
| Non Proprietary Name: | BENZOCAINE |
| Active Ingredient(s): | 20 g/100g & nbsp; BENZOCAINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37205-122 |
| Labeler Name: | CARDINAL HEALTH |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120501 |
| Package NDC: | 37205-122-12 |
| Package Description: | 1 TUBE in 1 CARTON (37205-122-12) > 20 g in 1 TUBE |
| NDC Code | 37205-122-12 |
| Proprietary Name | LEADER ORAL ANALGESIC |
| Package Description | 1 TUBE in 1 CARTON (37205-122-12) > 20 g in 1 TUBE |
| Product NDC | 37205-122 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZOCAINE |
| Dosage Form Name | GEL |
| Route Name | ORAL |
| Start Marketing Date | 20120501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CARDINAL HEALTH |
| Substance Name | BENZOCAINE |
| Strength Number | 20 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |