FDA.reportPublic FDA data

Global Household Antibacterial Lemon Fresh Scent

Manufacturer
TARGET PRICE, INC.
Effective date
2020-09-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:10

Label at a glance#

ProductGlobal Household Antibacterial Lemon Fresh Scent
Active ingredientCHLOROXYLENOL
Label structure7 sections

Dosage and administration

Wet hands and forearms. Apply 5 ml or palmfu to hands and forearms. Scrub thoroughly for 30 seconds and rinse.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.30%

Purpose

OTC - PURPOSE SECTION

Antibacterial hand soap

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Keep Out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, drink a glass of water to dilute. if eye contact occurs, rinse thoroughly with water.

Directions.

DOSAGE & ADMINISTRATION SECTION

Wet hands and forearms. Apply 5 ml or palmfu to hands and forearms. Scrub thoroughly for 30 seconds and rinse.

Inactive ingredients.

INACTIVE INGREDIENT SECTION

water, sodium, lauril sulfate, lauramine oxide, sodium laureth sulfate, alcoholdenat., phenoxyethanol, sodium chloride, PPG-26, PEI-14 PGE24/PPG-16 copolymer, sodium hydroxide, fragrance, C9-11, pareth-8, tetrasodium glumate diacetate, yellow 5, methylisothiazoinone, blue 1

Package Labeling:354.88ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle5Bottle5

Package Labeling:739.33ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle6Bottle6

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
72146-04372146-043-00, 72146-043-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM9NEZ333N27IACT
LAURYL SULFATEDIQ16UC154IACT
LAURAMINE OXIDE4F6FC4MI8WIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
ALCOHOL3K9958V90MIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM CHLORIDE451W47IQ8XIACT
PPG-26V86KZL3H2ZIACT
SODIUM HYDROXIDE55X04QC32IIACT
C9-11 PARETH-880E6PSE1XLIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
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
d127643b-e00c-8033-e053-2a95a90adfdaae811f48-e2e1-7fee-e053-2a95a90afbb52021-11-19WarningsExact identifier
spl set id: ae811f48-e2e1-7fee-e053-2a95a90afbb5

Reported adverse events (FAERS/openFDA)#

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