Product NDC: | 61734-102 |
Proprietary Name: | Hand Sanitizer |
Non Proprietary Name: | Benzethonium |
Active Ingredient(s): | .2 mg/100mL & nbsp; Benzethonium |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61734-102 |
Labeler Name: | Delon Laboratories (1990) Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100520 |
Package NDC: | 61734-102-02 |
Package Description: | 8 mL in 1 BOTTLE, SPRAY (61734-102-02) |
NDC Code | 61734-102-02 |
Proprietary Name | Hand Sanitizer |
Package Description | 8 mL in 1 BOTTLE, SPRAY (61734-102-02) |
Product NDC | 61734-102 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzethonium |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100520 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Delon Laboratories (1990) Ltd |
Substance Name | BENZETHONIUM CHLORIDE |
Strength Number | .2 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |