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Clario Free Foaming Hand Sanitizer
Clario Free Foaming Hand Sanitizer - 65601-778-29 - (Benzalkonium Chloride)
Drug Information of Clario Free Foaming Hand Sanitizer
| Product NDC: | 65601-778 |
| Proprietary Name: | Clario Free Foaming Hand Sanitizer |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | 1.3 mg/mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOAP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clario Free Foaming Hand Sanitizer
| Product NDC: | 65601-778 |
| Labeler Name: | Betco Corporation, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121112 |
Package Information of Clario Free Foaming Hand Sanitizer
| Package NDC: | 65601-778-29 |
| Package Description: | 1000 mL in 1 BAG (65601-778-29) |
NDC Information of Clario Free Foaming Hand Sanitizer
| NDC Code | 65601-778-29 |
| Proprietary Name | Clario Free Foaming Hand Sanitizer |
| Package Description | 1000 mL in 1 BAG (65601-778-29) |
| Product NDC | 65601-778 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | SOAP |
| Route Name | TOPICAL |
| Start Marketing Date | 20121112 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Betco Corporation, Ltd. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | 1.3 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
