HAND SANITISER FOAM- benzalonium chloride liquid SANITIZINGSOAP- benzalonium chloride liquid HAND SANITIZER GEL- benzalonium chloride liquid
Hand sanitizer gel by
Drug Labeling and Warnings
Hand sanitizer gel by is a Otc medication manufactured, distributed, or labeled by Landy International. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HAND SANITISER FOAM
benzalonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 51706-807 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 13 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 96.59 mL in 100 mL POLIHEXANIDE (UNII: 322U039GMF) 0.26 mL in 100 mL TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B) 0.74952 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 51706-807-01 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2020 2 NDC: 51706-807-02 244 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2020 3 NDC: 51706-807-03 1200 mL in 1 BAG; Type 0: Not a Combination Product 06/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/01/2020 SANITIZINGSOAP
benzalonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 51706-806 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 10 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 80.6 mL in 100 mL LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233) 12 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL in 100 mL BENZYL ALCOHOL (UNII: LKG8494WBH) 1 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 51706-806-01 1200 mL in 1 BAG; Type 0: Not a Combination Product 06/01/2020 2 NDC: 51706-806-02 244 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2020 3 NDC: 51706-806-03 3780 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/01/2020 HAND SANITIZER GEL
benzalonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC: 51706-808 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 13 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) 96.59 mL in 100 mL POLIHEXANIDE (UNII: 322U039GMF) 0.26 mL in 100 mL TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B) 0.74952 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 51706-808-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/01/2020 2 NDC: 51706-808-02 90 mL in 1 BOX; Type 0: Not a Combination Product 06/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/01/2020 Labeler - Landy International (545291775) Establishment Name Address ID/FEI Business Operations Landy International 545291775 manufacture(51706-806, 51706-807, 51706-808)
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