Product NDC: | 21749-700 |
Proprietary Name: | PURELL Advanced Instant Hand Sanitizer |
Non Proprietary Name: | ALCOHOL |
Active Ingredient(s): | .7 mL/mL & nbsp; ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21749-700 |
Labeler Name: | GOJO Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110510 |
Package NDC: | 21749-700-60 |
Package Description: | 60 mL in 1 BOTTLE (21749-700-60) |
NDC Code | 21749-700-60 |
Proprietary Name | PURELL Advanced Instant Hand Sanitizer |
Package Description | 60 mL in 1 BOTTLE (21749-700-60) |
Product NDC | 21749-700 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALCOHOL |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20110510 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | GOJO Industries, Inc. |
Substance Name | ALCOHOL |
Strength Number | .7 |
Strength Unit | mL/mL |
Pharmaceutical Classes |