Product NDC: | 53329-976 |
Proprietary Name: | Skintegrity Foaming Hand Sanitizer |
Non Proprietary Name: | Benzethonium Chloride |
Active Ingredient(s): | .2 mL/100mL & nbsp; Benzethonium Chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53329-976 |
Labeler Name: | Medline Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110408 |
Package NDC: | 53329-976-84 |
Package Description: | 1000 mL in 1 BAG (53329-976-84) |
NDC Code | 53329-976-84 |
Proprietary Name | Skintegrity Foaming Hand Sanitizer |
Package Description | 1000 mL in 1 BAG (53329-976-84) |
Product NDC | 53329-976 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzethonium Chloride |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20110408 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Medline Industries, Inc. |
Substance Name | BENZETHONIUM CHLORIDE |
Strength Number | .2 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |