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KLEENEX Luxury Foam Hand Sanitizer
KLEENEX Luxury Foam Hand Sanitizer - 55118-521-10 - (Benzalkonium Chloride)
Drug Information of KLEENEX Luxury Foam Hand Sanitizer
| Product NDC: | 55118-521 |
| Proprietary Name: | KLEENEX Luxury Foam Hand Sanitizer |
| Non Proprietary Name: | Benzalkonium Chloride |
| Active Ingredient(s): | .001 g/mL & nbsp; Benzalkonium Chloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KLEENEX Luxury Foam Hand Sanitizer
| Product NDC: | 55118-521 |
| Labeler Name: | Kimberly-Clark Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110815 |
Package Information of KLEENEX Luxury Foam Hand Sanitizer
| Package NDC: | 55118-521-10 |
| Package Description: | 1000 mL in 1 CONTAINER (55118-521-10) |
NDC Information of KLEENEX Luxury Foam Hand Sanitizer
| NDC Code | 55118-521-10 |
| Proprietary Name | KLEENEX Luxury Foam Hand Sanitizer |
| Package Description | 1000 mL in 1 CONTAINER (55118-521-10) |
| Product NDC | 55118-521 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzalkonium Chloride |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110815 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kimberly-Clark Corporation |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .001 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
