Product NDC: | 50225-355 |
Proprietary Name: | Instant Hand Sanitizer |
Non Proprietary Name: | Instant Hand Sanitizer |
Active Ingredient(s): | 60 g/mL & nbsp; Instant Hand Sanitizer |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50225-355 |
Labeler Name: | Global Protection USA, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100106 |
Package NDC: | 50225-355-01 |
Package Description: | 59 mL in 1 BOTTLE (50225-355-01) |
NDC Code | 50225-355-01 |
Proprietary Name | Instant Hand Sanitizer |
Package Description | 59 mL in 1 BOTTLE (50225-355-01) |
Product NDC | 50225-355 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Instant Hand Sanitizer |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100106 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Global Protection USA, Inc. |
Substance Name | ALCOHOL |
Strength Number | 60 |
Strength Unit | g/mL |
Pharmaceutical Classes |