Product NDC: | 21749-740 |
Proprietary Name: | PURELL Advanced Hand Sanitizer Ocean Kiss |
Non Proprietary Name: | alcohol |
Active Ingredient(s): | .7 mL/mL & nbsp; alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21749-740 |
Labeler Name: | GOJO Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20111221 |
Package NDC: | 21749-740-01 |
Package Description: | 29 mL in 1 BOTTLE (21749-740-01) |
NDC Code | 21749-740-01 |
Proprietary Name | PURELL Advanced Hand Sanitizer Ocean Kiss |
Package Description | 29 mL in 1 BOTTLE (21749-740-01) |
Product NDC | 21749-740 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | alcohol |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20111221 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | GOJO Industries, Inc. |
Substance Name | ALCOHOL |
Strength Number | .7 |
Strength Unit | mL/mL |
Pharmaceutical Classes |