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 |