| Product NDC: | 42739-001 |
| Proprietary Name: | CliniStat Pain Relieving |
| Non Proprietary Name: | BENZOCAINE,MENTHOL |
| Active Ingredient(s): | 20; .5 g/100g; g/100g & nbsp; BENZOCAINE,MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42739-001 |
| Labeler Name: | TheraBrands |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120222 |
| Package NDC: | 42739-001-00 |
| Package Description: | 28 g in 1 CAN (42739-001-00) |
| NDC Code | 42739-001-00 |
| Proprietary Name | CliniStat Pain Relieving |
| Package Description | 28 g in 1 CAN (42739-001-00) |
| Product NDC | 42739-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZOCAINE,MENTHOL |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20120222 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | TheraBrands |
| Substance Name | BENZOCAINE; MENTHOL |
| Strength Number | 20; .5 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |