FDA.reportPublic FDA data

Lyrall Citrus Burst Antibacterial Liquid HandSoap

Manufacturer
Mekor LLC
Effective date
2021-12-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:22:34

Label at a glance#

ProductLyrall Citrus Burst Antibacterial Liquid HandSoap
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For handwashing to decrease the bacteria on the skin.

Dosage and administration

• Pump into hands, wet as needed • Lather vigorously for at least 20 seconds. • Wash skin, rinse thoroughly and dry

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease the bacteria on the skin.

Warnings

WARNINGS SECTION

For External Use Only
When using the product • Avoid contact with eyes. In case of eye contact, flush with water.
Stop use and ask a doctor if irritation or rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

• Pump into hands, wet as needed • Lather vigorously for at least 20 seconds. • Wash skin, rinse thoroughly and dry

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Aqua (Water, Eau), Disodium EDTA, Glycerin, Sodium Lauryl Ether Sulfate, Cocamide MEA, Cocamidopropyl Betaine, Aloe Barbadensis Leaf Extract, Methylisothiazolinone and Methylchloroisothiazolinone, Citrus Aurantifolia (Lime) Oil, Citric Acid, Sodium Chloride, Fragrance and CI 47005 (Yellow 10).

Questions? 

OTC - QUESTIONS SECTION

1-888- 495-3978

SPL UNCLASSIFIED SECTION

KILLS 99.9% BACTERIA

- WITH ALOE VERA & ESSENTIAL OILS -

moisturizing 

pH balanced • paraben-free 

gentle cleanser

Distributed by:
Mekor Corp
One Rockefeller Plaza, 11th Floor
New York, NY 10020
www.lyrall.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77679-10277679-102-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
GLYCERINPDC6A3C0OXIACT
SODIUM LAURETH-3 SULFATEBPV390UAP0IACT
COCO MONOETHANOLAMIDEC80684146DIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
ALOE VERA LEAFZY81Z83H0XIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
LIME OIL, COLD PRESSEDUZH29XGA8GIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM CHLORIDE451W47IQ8XIACT
D&C YELLOW NO. 1035SW5USQ3GIACT

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
e4e1d13b-b452-4811-9617-5b36fbb01997fc8f8570-f416-4721-a5e8-3d2bbdd48abf2021-12-15WarningsExact identifier
spl id: e4e1d13b-b452-4811-9617-5b36fbb01997
spl set id: fc8f8570-f416-4721-a5e8-3d2bbdd48abf

Reported adverse events (FAERS/openFDA)#

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