Hand sanitizer gel

Manufacturer
Landy International
Effective date
2020-06-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:27:31

Label at a glance#

ProductHand sanitiser foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure5 sections

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

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

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Benzalkonium Chloride 0.1%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 51706-806 806 package806 package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

51706-807 NDC 807 package807 package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

51706-808 NDC 808808

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51706-806-012024-06-12C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-806-022024-06-12C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-806-032024-06-12C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-807-012024-06-12C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-807-022024-06-12C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-807-032024-06-12C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-808-012024-06-12C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-808-022024-06-12C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-806-012022-01-28C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-806-022022-01-28C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-806-032022-01-28C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-807-012022-01-28C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-807-022022-01-28C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-807-032022-01-28C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-808-012022-01-28C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570
51706-808-022022-01-28C16284748780-1d6a99b39-8dda-a426-e053-dadaa90af4c2a768f84a-25c8-5d04-e053-2a95a90a5570

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1aadfcac-0f94-7a90-e063-6394a90af911a768f84a-25c8-5d04-e053-2a95a90a55702024-06-12Exact identifier
spl set id: a768f84a-25c8-5d04-e053-2a95a90a5570

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.