FDA.reportPublic FDA data

Truth Alcohol Free Hand Sanitizer - Lavender Eucalyptus

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 22:02:28

Label at a glance#

ProductTruth Alcohol Free Hand Sanitizer - Lavender Eucalyptus
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 a small amount of product into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly for 15 seconds until dry.

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, or if conditions persist for more than 72 hours

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 a small amount of product into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly for 15 seconds until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, Citric Acid, Fragrance.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73126-03373126-033-01, 73126-033-02, 73126-033-03, 73126-033-04, 73126-033-05, 73126-033-06, 73126-033-07, 73126-033-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
GLYCERETH-17 COCOATE3057VPT0KCIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
dd944506-1dcc-402b-e053-2a95a90a343047ff6324-c822-4fd2-b248-911bcac0b2e32022-04-26WarningsExact identifier
spl id: dd944506-1dcc-402b-e053-2a95a90a3430
spl set id: 47ff6324-c822-4fd2-b248-911bcac0b2e3

Reported adverse events (FAERS/openFDA)#

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