| Product NDC: | 48871-009 |
| Proprietary Name: | Crayola Sunglow Yellow Roll On Hand Sanitizer |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | .0013 mL/mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 48871-009 |
| 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: | 48871-009-01 |
| Package Description: | 4 CARTON in 1 CASE (48871-009-01) > 6 BLISTER PACK in 1 CARTON > 1 BOTTLE in 1 BLISTER PACK > 20 mL in 1 BOTTLE |
| NDC Code | 48871-009-01 |
| Proprietary Name | Crayola Sunglow Yellow Roll On Hand Sanitizer |
| Package Description | 4 CARTON in 1 CASE (48871-009-01) > 6 BLISTER PACK in 1 CARTON > 1 BOTTLE in 1 BLISTER PACK > 20 mL in 1 BOTTLE |
| Product NDC | 48871-009 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | GEL |
| 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 |