| 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 |