Lysol

Manufacturer
Reckitt Benckiser LLC
Effective date
2011-12-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:49:57

Label at a glance#

ProductLysol No Touch
Active ingredientBenzethonium chloride
Label structure10 sections

Dosage and administration

Wet hands. Place hands under dispenser until soap is dispensed. Wash hands. Rinse hands with water. Dry hands after rinsing.

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzethonium chloride, 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product:

  • Avoid contact with eyes.
  • In case of eye contact, flush with water.

OTC - ASK DOCTOR SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands.
  • Place hands under dispenser until soap is dispensed.
  • Wash hands.
  • Rinse hands with water.
  • Dry hands after rinsing.

Other Information

STORAGE AND HANDLING SECTION

store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Cetrimonium Chloride, Lauramide DEA, PEG-150 Distearate, Lauramine Oxide, Fragrance, Citric Acid, Tetrasodium EDTA, Benzophenone-4, Di-PPG-2 Myreth-10 Adipate, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Blue 1 and D&C Red 33.

Questions? Comments?

OTC - QUESTIONS SECTION

Call 1-800-228-4722

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lysol®
BRAND
KILLS 99.9% OF BACTERIA

No -Touch™
Antibacterial
Hand Soap

No -Touch™
Hand Soap System

Winterberry Sparkle
includes dispenser, hand soap refill and AA batteries

Helps stop the
spread of bacteria

8.5 FL. OZ.
(251 mL)

Principal Display Panel - 251 mL Bottle Label
Principal Display Panel - 251 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Benzethonium chlorideACTIVE INGREDIENTPH41D057441
BenzethoniumACTIVE MOIETY1VU15B70BP1

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
63824-45263824-452-01, 63824-452-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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
fceed9bd-452f-0afc-e053-6394a90a1ed6755bc422-3ea4-4ca6-8a47-1ba67e4c145c2023-05-30WarningsExact identifier
spl set id: 755bc422-3ea4-4ca6-8a47-1ba67e4c145c

Reported adverse events (FAERS/openFDA)#

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