Product NDC: | 50593-008 |
Proprietary Name: | Clinical Works Ocean Breeze Waterless Hand Sanitizer |
Non Proprietary Name: | Alcohol |
Active Ingredient(s): | 62 g/100g & nbsp; Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50593-008 |
Labeler Name: | Taizhou Xinzhixuan Daily-Use Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100610 |
Package NDC: | 50593-008-01 |
Package Description: | 60 g in 1 BOTTLE (50593-008-01) |
NDC Code | 50593-008-01 |
Proprietary Name | Clinical Works Ocean Breeze Waterless Hand Sanitizer |
Package Description | 60 g in 1 BOTTLE (50593-008-01) |
Product NDC | 50593-008 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Alcohol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100610 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Taizhou Xinzhixuan Daily-Use Co., Ltd. |
Substance Name | ALCOHOL |
Strength Number | 62 |
Strength Unit | g/100g |
Pharmaceutical Classes |