FDA.reportPublic FDA data

Lysol

Manufacturer
Reckitt Benckiser LLC
Effective date
2015-01-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:29:13

Label at a glance#

ProductLysol Touch of Foam
Active ingredientBenzalkonium Chloride
Label structure11 sections

Indications and uses

for handwashing to decrease bacteria on the skin

Dosage and administration

Apply product to hands. Wash hands. Rinse hands with water.

Storage and handling

store at room temperature

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.10%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE 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

  • Apply product to hands.
  • Wash hands.
  • Rinse hands with water.

Other Information

STORAGE AND HANDLING SECTION

store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Lauramine Oxide, PEG-150 Distearate, Cetrimonium Chloride, Propylene Glycol, Fragrance, Citric Acid, Tetrasodium EDTA, Cocamide MEA, Hydrolyzed Collagen, Magnesium Nitrate, Butylene Glycol, Phenoxyethanol, Methylchloroisothiazolinone, Magnesium Chloride, Ethylhexylglycerin, Methylisothiazolinone, D&C Orange 4.

Questions? Comments?

OTC - QUESTIONS SECTION

Call 1-800-228-4722

SPL UNCLASSIFIED SECTION

Distributed by:
Reckitt Benckiser
Parsippany, NJ 07054-0224

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW FORMULA!

Lysol®
BRAND
KILLS 99.9% OF BACTERIA

Soft on Skin,
HARD ON GERMS®

Antibacterial
Foam Hand Wash

with
MOISTURIZING
COLLAGEN
COMPLEX

8.5 FL. OZ.
(251 mL)

Soothing Honey & Milk

8170202

PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63824-483-012023-11-15C16284748780-19d75b9d0-b72b-f424-e053-dadaa90a57ceLysol ® Touch of Foam
63824-483-012020-01-31C16284748780-19d75b9d0-b72b-f424-e053-dadaa90a57ceLysol ® Touch of Foam

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63824-48363824-483-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
Benzalkonium ChlorideF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
COCO MONOETHANOLAMIDEC80684146DIACT
MAGNESIUM NITRATE77CBG3UN78IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
PHENOXYETHANOLHIE492ZZ3TIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
MAGNESIUM CHLORIDE02F3473H9OIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
D&C ORANGE NO. 4Q1LIY3BO0UIACT

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
0a3a98dc-9b23-9f29-e063-6394a90a4eb998541bbb-7cb5-4339-ae35-c19049cdb0ef2023-11-15WarningsExact identifier
spl set id: 98541bbb-7cb5-4339-ae35-c19049cdb0ef

Reported adverse events (FAERS/openFDA)#

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