FDA.reportPublic FDA data

154 Antibacterial Liquid Hand

Manufacturer
Worklife Brands, LLC
Effective date
2025-09-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:12:26

Label at a glance#

Product154 Antibacterial Liquid Hand
Active ingredientCHLOROXYLENOL
Label structure9 sections

Indications and uses

Handwash to help decrease bacteria on the skin. / Lavado de manos para ayudar a disminuir las bacterias en la piel.

Dosage and administration

• Apply a small amount of product to wet hands, work into lather for 30 seconds, and rinse thoroughly. / Aplique una pequeña cantidad de producto en las manos mojadas, haga espuma durante 30 segundos y enjuague bien. • Children under 6 years of age should be supervised when using this product. / Los niños menores de 6 años deben ser supervisados cuando utilicen este producto.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT / INGREDIENTE ACTIVO

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.1% / Cloroxilenol al 0.1%

PURPOSE / OBJETIVO

OTC - PURPOSE SECTION

Antiseptic / Antiséptico

USES / USOS

INDICATIONS & USAGE SECTION

Handwash to help decrease bacteria on the skin. / Lavado de manos para ayudar a disminuir las bacterias en la piel.

WARNINGS / ADVERTENCIAS

WARNINGS SECTION

FOR EXTERNAL USE ONLY. / ÚNICAMENTE PARA USO EXTERNO.

DO NOT USE in the eyes. In case of contact, immediately flush eyes with water.
NO USAR en los ojos. En caso de contacto, enjuagar inmediatamente con agua .

OTC - ASK DOCTOR SECTION

STOP USE AND ASK A DOCTOR IF irritation or rash appears and lasts.

DEJE DE USARLO Y CONSULTE A UN MÉDICO SI aparece irritación o sarpullido y persiste.

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.

MANTENER FUERA DEL ALCANCE DE LOS NIÑOS. En caso de ingestión, busque ayuda médica o comuníquese
con un centro de control de intoxicaciones de inmediato.

DIRECTIONS / INSTRUCCIONES:

DOSAGE & ADMINISTRATION SECTION

• Apply a small amount of product to wet hands, work into lather for 30 seconds, and rinse thoroughly. / Aplique
una pequeña cantidad de producto en las manos mojadas, haga espuma durante 30 segundos y enjuague bien.
• Children under 6 years of age should be supervised when using this product. / Los niños menores de 6 años
deben ser supervisados cuando utilicen este producto.

INACTIVE INGREDIENTS / INGREDIENTES INACTIVOS:

INACTIVE INGREDIENT SECTION

Water (Agua) (7732-18-5), Sodium C14-16 Olefin Sulfonate (Sulfonato de olefina C14-16 de sodio)
(68439-57-6), Cocamidopropyl Hydroxysultaine (Cocamidopropil hidroxisultaína) (68139-30-0), Sodium
Chloride (Cloruro de sodio) (7647-14-5), Propanediol (Propanodiol) (26264-14-2), Propylene Glycol
(Propilenglicol) (57-55-6), Sodium Polyitaconate (Politaconato de sodio) (26099-89-8), Fragrance (Proprietary)
(Fragancia (Propietaria)), 2-Bromo-2-Nitropropane-1,3-Diol (-bromo-2-nitropropano-1,3-diol) (52-51-7),
Methylisothiazolinone (Metilisotiazolinona) (2682-20-4), Methylchloroisothiazolinone (Metilcloroisotiazolinona)
(26172-55-4), Yellow 5 (Amarillo 5) (1934-21-0), Red 40 (Rojo 40) (25956-17-6).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal DisplayPrincipal Display

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1941461chloroxylenol 0.1 % Medicated Liquid SoapPSN1
1941461chloroxylenol 1 MG/ML Medicated Liquid SoapSCD1
1941461chloroxylenol 0.1 % Medicated Liquid SoapSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80434-701-41154 Antibacterial Liquid Hand3.78 L in 1 BOTTLE, PLASTICSOAP3.781

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
80434-70180434-701-41

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
CHLOROXYLENOL0F32U78V2QACTIB
FD&C RED NO. 40WZB9127XOAIACT
PROPANEDIOL5965N8W85TIACT
SODIUM POLYITACONATE (2800 MW, PHOSPHATE TERMINATED)G7SW5QN7TTIACT
BRONOPOL6PU1E16C9WIACT
WATER059QF0KO0RIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
SODIUM CHLORIDE451W47IQ8XIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT

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
154 Antibacterial Liquid HandCHLOROXYLENOLWorklife Brands, LLC3de748aa-6dd8-470b-e063-6394a90a2e8e2025-09-03WarningsExact identifier
ndc (package): 80434-701-41
ndc (product): 80434-701
ndc11 (package): 80434070141
spl id: 3de748aa-6dd9-470b-e063-6394a90a2e8e
spl set id: 3de748aa-6dd8-470b-e063-6394a90a2e8e

Reported adverse events (FAERS/openFDA)#

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