- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- nonalcohol
-
INGREDIENTS AND APPEARANCE
HAND SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:19392-120 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 g in 1000 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5) GLYCERETH-17 COCOATE (UNII: 3057VPT0KC) LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:19392-120-01 8 g in 1 BOTTLE, PLASTIC 2 NDC:19392-120-03 30 g in 1 BOTTLE, PLASTIC 3 NDC:19392-120-04 50 g in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 07/02/2014 Labeler - Humphreyline (122539042)