Product NDC: | 68609-575 |
Proprietary Name: | Sani-Foam Instant Hand Sanitizer |
Non Proprietary Name: | BENZETHONIUM CHLORIDE |
Active Ingredient(s): | 2 mg/mL & nbsp; BENZETHONIUM CHLORIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68609-575 |
Labeler Name: | General Products & Supply, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20040131 |
Package NDC: | 68609-575-55 |
Package Description: | 208200 mL in 1 DRUM (68609-575-55) |
NDC Code | 68609-575-55 |
Proprietary Name | Sani-Foam Instant Hand Sanitizer |
Package Description | 208200 mL in 1 DRUM (68609-575-55) |
Product NDC | 68609-575 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZETHONIUM CHLORIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20040131 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | General Products & Supply, Inc. |
Substance Name | BENZETHONIUM CHLORIDE |
Strength Number | 2 |
Strength Unit | mg/mL |
Pharmaceutical Classes |