FDA.reportPublic FDA data

Family Dollar Antibacterial Hand

Manufacturer
Family Dollar Services, Inc
Effective date
2017-12-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:05:57

Label at a glance#

ProductFamily Dollar Antibacterial Hand
Active ingredientBENZETHONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Wet hands, work into a rich lather • Rinse well.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzethonium Chloride 0.10%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Handwashing to decrease bacteria on skin

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develop or increase.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands, work into a rich lather • Rinse well.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Sodium Laureth Sulfate, Sodium Chloride, Ammonium Lauryl Sulfate, Cocamidopropyl Betaine, Parfum (Fragrance), PEG-150 Distearate, Glycerin, Methylchloroisothiazolinone, Methylisothiazolinone, Hydrogenated Castor Oil, Tetrasodium EDTA, Citric Acid, Lauramine Oxide, Sodium Benzoate, Butylphenyl Methylpropianol, Amyl Cinnamal, Coumarin, Eugenol, Linalool, Yellow 5, Red 4.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55319-95055319-950-01, 55319-950-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM CHLORIDE451W47IQ8XIACT
AMMONIUM LAURYL SULFATEQ7AO2R1M0BIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
GLYCERINPDC6A3C0OXIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
EDETATE SODIUMMP1J8420LUIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
SODIUM BENZOATEOJ245FE5EUIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
.ALPHA.-AMYLCINNAMALDEHYDEWC51CA3418IACT
COUMARINA4VZ22K1WTIACT
EUGENOL3T8H1794QWIACT
LINALOOL, (+/-)-D81QY6I88EIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C RED NO. 4X3W0AM1JLXIACT
BENZETHONIUM CHLORIDEPH41D05744ACTIB

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
d29a6b77-6869-6a94-e053-2a95a90a34204639eb2c-6f3a-00ac-e054-00144ff88e882021-12-07WarningsExact identifier
spl set id: 4639eb2c-6f3a-00ac-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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