FDA.reportPublic FDA data

Lemongrass Antimicrobial

Manufacturer
Sanit Technologies LLC | Sanit Technologies LLC dba Durisan
Effective date
2021-08-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:37:06

Label at a glance#

ProductLemongrass Antimicrobial
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Pump onto dry skin. Lather vigorously for 15 seconds. Rinse and dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.When using this product, avoid contact with eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if irritation or redness develops.

Keep out of reach of children except under adult supervision. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump onto dry skin. Lather vigorously for 15 seconds. Rinse and dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, cocamidopropyl betaine, glycerin, cetrimonium chloride, benzyl alcohol, disodium EDTA, fragrance, benzoic acid, sorbic acid, citric acid, Yellow 5 (CI 19140), sodium chloride.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71120-11871120-118-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
GLYCERINPDC6A3C0OXIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
BENZYL ALCOHOLLKG8494WBHIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
BENZOIC ACID8SKN0B0MIMIACT
SORBIC ACIDX045WJ989BIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM CHLORIDE451W47IQ8XIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
cadfd26a-72eb-0920-e053-2995a90a04ea347eedf9-97b6-4f68-a6ee-0e322804d0622021-08-31WarningsExact identifier
spl id: cadfd26a-72eb-0920-e053-2995a90a04ea
spl set id: 347eedf9-97b6-4f68-a6ee-0e322804d062

Reported adverse events (FAERS/openFDA)#

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