FDA.reportPublic FDA data

FRENCH LAVENDER HOME

Manufacturer
HOME & BODY COMPANY
Effective date
2022-01-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:10:52

Label at a glance#

ProductFRENCH LAVENDER HOME
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Wash hands and rinse

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride  0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

Help eliminate bacteria on hands

Warnings

WARNINGS SECTION

For external use only.

When using this product do not use in or near the eyes.
In case of contact, rinse eyes throughly with water.

OTC - STOP USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children, except under adult supervision. If swallowed, get medical help or  contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wash hands and rinse

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Chloride, Sodium Benzoate, Phenoxyethanol, Polysorbate 20, Fragrance, Glycerin

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73746-003-012022-01-31C16284748780-1d6a99b39-ef5d-a426-e053-dadaa90af4c2FRENCH LAVENDER ANTIBACTERIAL HOME SOAP
73746-003-012022-01-28C16284748780-1d6a99b39-ef5d-a426-e053-dadaa90af4c2FRENCH LAVENDER ANTIBACTERIAL HOME SOAP

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73746-00373746-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM BENZOATEOJ245FE5EUIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYSORBATE 207T1F30V5YHIACT
GLYCERINPDC6A3C0OXIACT
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
ea531ea0-29b7-161e-e053-2995a90a08bbfd9ffe5a-edbf-46eb-be9b-fca4c1ce10d12022-10-05WarningsExact identifier
spl set id: fd9ffe5a-edbf-46eb-be9b-fca4c1ce10d1

Reported adverse events (FAERS/openFDA)#

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