HAND SANITISER FOAM- benzalonium chloride liquid 
SANITIZINGSOAP- benzalonium chloride liquid 
HAND SANITIZER GEL- benzalonium chloride liquid 
Landy International

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Purified water，Benzalkonium Chloride，TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE， Polyaminopropyl biguanide hcl

Benzalkonium Chloride 0.13%

Benzalkonium Chloride 0.1%

NDC 51706-806 806 package

51706-807 NDC 807 package

51706-808 NDC 808

HAND SANITISER FOAM 
benzalonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51706-807
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51706-807-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
2NDC:51706-807-02244 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
3NDC:51706-807-031200 mL in 1 BAG; Type 0: Not a Combination Product06/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)06/01/202008/31/2020
SANITIZINGSOAP 
benzalonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51706-806
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE10 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51706-806-011200 mL in 1 BAG; Type 0: Not a Combination Product06/01/2020
2NDC:51706-806-02244 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
3NDC:51706-806-033780 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)06/01/202008/31/2020
HAND SANITIZER GEL 
benzalonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51706-808
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE13 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51706-808-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
2NDC:51706-808-0290 mL in 1 BOX; Type 0: Not a Combination Product06/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)06/01/202008/31/2020
Labeler - Landy International (545291775)
Establishment
NameAddressID/FEIBusiness Operations
Landy International545291775manufacture(51706-806, 51706-807, 51706-808)

Revised: 6/2024
Document Id: 1aadfcac-0f94-7a90-e063-6394a90af911
Set id: a768f84a-25c8-5d04-e053-2a95a90a5570
Version: 2
Effective Time: 20240612
 
Landy International