Product NDC: | 48871-005 |
Proprietary Name: | Crayola Hand Sanitizing Foam |
Non Proprietary Name: | benzalkonium chloride |
Active Ingredient(s): | .0013 mL/mL & nbsp; benzalkonium chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 48871-005 |
Labeler Name: | Health-Tech, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100901 |
Package NDC: | 48871-005-01 |
Package Description: | 12 BOTTLE, PUMP in 1 CASE (48871-005-01) > 9 mL in 1 BOTTLE, PUMP |
NDC Code | 48871-005-01 |
Proprietary Name | Crayola Hand Sanitizing Foam |
Package Description | 12 BOTTLE, PUMP in 1 CASE (48871-005-01) > 9 mL in 1 BOTTLE, PUMP |
Product NDC | 48871-005 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | benzalkonium chloride |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20100901 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Health-Tech, Inc. |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | .0013 |
Strength Unit | mL/mL |
Pharmaceutical Classes |