FDA.reportPublic FDA data

Life Quality Liquid

Manufacturer
LABORATORIOS ESME S.A.
Effective date
2022-11-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:49:53

Label at a glance#

ProductLife Quality Liquid
Active ingredientCHLOROXYLENOL
Label structure6 sections

Indications and uses

for hand washing to decrease bacteria on the skin.

Dosage and administration

wet hands as needed lather vigorously for at least 15 seconds rinse and dry thoroughly.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • for hand washing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact ith eyes. In case of contact eye, flush with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops.

Do not use

OTC - DO NOT USE SECTION

in children under 3 years old.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Do not swallow.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands as needed
  • lather vigorously for at least 15 seconds
  • rinse and dry thoroughly.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Aqua, Sodium Laureth Sulfate, Sodium Chloride, Cocamidopropyl Betaine, Styrene Butadiene Copolymer, Citric Acid, Fragrance, Salicylic Acid, Glycerin, Polyquaternium-7, Sodium Hydroxide, Disodium EDTA, Methylisothiazolinone/Methylchloroisothiazolinone.

Package Labeling:250ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

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
81349-00181349-001-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM CHLORIDE451W47IQ8XIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SALICYLIC ACIDO414PZ4LPZIACT
GLYCERINPDC6A3C0OXIACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)0L414VCS5YIACT
SODIUM HYDROXIDE55X04QC32IIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
CHLOROXYLENOL0F32U78V2QACTIB

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
ec82d308-8b36-6761-e053-2a95a90ae6edb865707f-3877-a4d5-e053-2a95a90aab402022-11-02WarningsExact identifier
spl id: ec82d308-8b36-6761-e053-2a95a90ae6ed
spl set id: b865707f-3877-a4d5-e053-2a95a90aab40

Reported adverse events (FAERS/openFDA)#

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