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KNOCKOUT
KNOCKOUT - 52490-200-17 - (Alcohol)
Drug Information of KNOCKOUT
| Product NDC: | 52490-200 |
| Proprietary Name: | KNOCKOUT |
| Non Proprietary Name: | Alcohol |
| Active Ingredient(s): | 42 mg/25mL & nbsp; Alcohol |
| Administration Route(s): | PERCUTANEOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KNOCKOUT
| Product NDC: | 52490-200 |
| Labeler Name: | Midway Advanced Products, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110801 |
Package Information of KNOCKOUT
| Package NDC: | 52490-200-17 |
| Package Description: | 50 PACKET in 1 CASE (52490-200-17) > 1.2 mL in 1 PACKET |
NDC Information of KNOCKOUT
| NDC Code | 52490-200-17 |
| Proprietary Name | KNOCKOUT |
| Package Description | 50 PACKET in 1 CASE (52490-200-17) > 1.2 mL in 1 PACKET |
| Product NDC | 52490-200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Alcohol |
| Dosage Form Name | SOLUTION |
| Route Name | PERCUTANEOUS |
| Start Marketing Date | 20110801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Midway Advanced Products, LLC |
| Substance Name | ALCOHOL |
| Strength Number | 42 |
| Strength Unit | mg/25mL |
| Pharmaceutical Classes |
