Product NDC: | 75887-001 |
Proprietary Name: | Hand Sanitizer |
Non Proprietary Name: | ALCOHOL |
Active Ingredient(s): | 5 mL/8mL & nbsp; ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75887-001 |
Labeler Name: | Aztex Enterprises |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110118 |
Package NDC: | 75887-001-05 |
Package Description: | 236 mL in 1 BOTTLE (75887-001-05) |
NDC Code | 75887-001-05 |
Proprietary Name | Hand Sanitizer |
Package Description | 236 mL in 1 BOTTLE (75887-001-05) |
Product NDC | 75887-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALCOHOL |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20110118 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Aztex Enterprises |
Substance Name | ALCOHOL |
Strength Number | 5 |
Strength Unit | mL/8mL |
Pharmaceutical Classes |