Product NDC: | 50730-8616 |
Proprietary Name: | Antiseptic Hand Gel |
Non Proprietary Name: | ethyl alcohol |
Active Ingredient(s): | .7 mL/mL & nbsp; ethyl alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50730-8616 |
Labeler Name: | H and P Industries, Inc. dba Triad Group |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19971117 |
Package NDC: | 50730-8616-5 |
Package Description: | 472 mL in 1 BOTTLE, PLASTIC (50730-8616-5) |
NDC Code | 50730-8616-5 |
Proprietary Name | Antiseptic Hand Gel |
Package Description | 472 mL in 1 BOTTLE, PLASTIC (50730-8616-5) |
Product NDC | 50730-8616 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ethyl alcohol |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 19971117 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | H and P Industries, Inc. dba Triad Group |
Substance Name | ALCOHOL |
Strength Number | .7 |
Strength Unit | mL/mL |
Pharmaceutical Classes |