Truth Antibacterial Foaming Hand Wash - Unscented

Manufacturer: LAB-CLEAN, INC
Effective date: 2022-04-26
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 22:02:25

Label at a glance#

ProductTruth Antibacterial Foaming Hand Wash - Unscented

Active ingredientBENZALKONIUM CHLORIDE

Label structure6 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

Apply small amount of product to wet hands. Work into lather and rub briskly for 15-30 seconds. Rinse thoroughly. Dry hands.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

When using this product, avoid contact with eyes. In case of eye contact flush eyes with water.Do not ingest.

Stop use and ask a doctor if irritation or redness develops and conditions persist.

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

Apply small amount of product to wet hands. Work into lather and rub briskly for 15-30 seconds. Rinse thoroughly. Dry hands.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Chloride, Cocamidopropyl Betaine, Lauramine Oxide, Disodium Cocoamphodipropionate, Glycerin, Methylchloroisothiazolinone.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Truth Antibacterial Foaming Hand Wash - Unscented
BENZALKONIUM CHLORIDE
WATER
SODIUM CHLORIDE
COCAMIDOPROPYL BETAINE
LAURAMINE OXIDE
DISODIUM COCOAMPHODIPROPIONATE
GLYCERIN
METHYLCHLOROISOTHIAZOLINONE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73126-032	73126-032-01, 73126-032-02, 73126-032-03, 73126-032-04, 73126-032-05, 73126-032-06, 73126-032-07, 73126-032-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
LAURAMINE OXIDE	4F6FC4MI8W	IACT
DISODIUM COCOAMPHODIPROPIONATE	6K8PRP397M	IACT
GLYCERIN	PDC6A3C0OX	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
dd944506-1db6-402b-e053-2a95a90a3430			001aa754-65e3-4c5a-91f5-71a3d809be0c	2022-04-26	Warnings	Exact identifier spl id: dd944506-1db6-402b-e053-2a95a90a3430 spl set id: 001aa754-65e3-4c5a-91f5-71a3d809be0c

Reported adverse events (FAERS/openFDA)#

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