Product NDC: | 29500-9088 |
Proprietary Name: | Hand Sanitizer |
Non Proprietary Name: | benzalkonium chloride |
Active Ingredient(s): | .27 mL/207mL & nbsp; benzalkonium chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 29500-9088 |
Labeler Name: | Personal Care Products |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110705 |
Package NDC: | 29500-9088-7 |
Package Description: | 207 mL in 1 BOTTLE, PLASTIC (29500-9088-7) |
NDC Code | 29500-9088-7 |
Proprietary Name | Hand Sanitizer |
Package Description | 207 mL in 1 BOTTLE, PLASTIC (29500-9088-7) |
Product NDC | 29500-9088 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | benzalkonium chloride |
Dosage Form Name | AEROSOL, FOAM |
Route Name | TOPICAL |
Start Marketing Date | 20110705 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Personal Care Products |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .27 |
Strength Unit | mL/207mL |
Pharmaceutical Classes |