NDC | 68604-237-01 |
Set ID | 2a1bc66d-cadb-4a27-bd74-e88c218670d6 |
Category | HUMAN OTC DRUG LABEL |
Packager | Auto-Chlor System, LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333E |
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HAND KLEEN FOAMING INSTANT HAND SANITIZER
benzethonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68604-237 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzethonium Chloride (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) Benzethonium Chloride 0.2 g in 100 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Propylene Glycol (UNII: 6DC9Q167V3) Phenoxyethanol (UNII: HIE492ZZ3T) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) Sodium Chloride (UNII: 451W47IQ8X) Glycerin (UNII: PDC6A3C0OX) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) Meadowfoamamidopropyl Betaine (UNII: HNV0L650LG) Lanolin (UNII: 7EV65EAW6H) Dimethicone (UNII: 92RU3N3Y1O) Disodium Laureth Sulfosuccinate (UNII: D6DH1DTN7E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68604-237-01 1000 mL in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/31/2012 Labeler - Auto-Chlor System, LLC (965194330) Establishment Name Address ID/FEI Business Operations Auto-Chlor System, LLC 965194330 manufacture(68604-237)