Product NDC: | 75997-011 |
Proprietary Name: | Vanilla Hand Sanitizer |
Non Proprietary Name: | ETHYL ALCOHOL |
Active Ingredient(s): | 62 mL/100mL & nbsp; ETHYL ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75997-011 |
Labeler Name: | Papermates, Inc. dba Noteworthy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110202 |
Package NDC: | 75997-011-01 |
Package Description: | 59 mL in 1 BOTTLE (75997-011-01) |
NDC Code | 75997-011-01 |
Proprietary Name | Vanilla Hand Sanitizer |
Package Description | 59 mL in 1 BOTTLE (75997-011-01) |
Product NDC | 75997-011 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ETHYL ALCOHOL |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20110202 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Papermates, Inc. dba Noteworthy |
Substance Name | ALCOHOL |
Strength Number | 62 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |