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 |