Dr Lift Antibacterial Hand Wash

Manufacturer
Spa de Soleil
Effective date
2026-04-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:55:46

Label at a glance#

ProductDr Lift Antibacterial Hand Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Apply to wet skin. Scrub thoroughly. Rinse and dry. Use as needed. Place enough product in the palm of your hands to thoroughly cover you hands. Rub hands together briskly until product is completely absorbed and hands are dry. Inactive Ingredients:

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13 %

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

Warnings

For external use only.

When using this product: If in eyes, rinse promptly and thoroughly with water. Discontinue use if irritation or redness develop.

Stop use and ask a doctor if irritation or redness occur for more than 72 hours.

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

INDICATIONS & USAGE SECTION

Apply to wet skin. Scrub thoroughly. Rinse and dry. Use as needed.

DOSAGE & ADMINISTRATION SECTION

Place enough product in the palm of your hands to thoroughly cover you hands. Rub hands together briskly until product is completely absorbed and hands are dry.

Inactive Ingredients:

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Sodium Chloride, Cocamidopropyl betaine, Aqua, Sodium Laureth Sulfate, Carbomer, Glycerin, *CO Humulus Lupulus (Hops) Extract, *CO Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, *CO Calendula Officinalis Flower Extract, *CO Chamomilla Recutita (Matricaria) Flower Extract, *CO Citrus Limon (Lemon) Peel Extract, *CO Cucumis Sativus (Cucumber) Seed Extract, *CO Camellia Sinensis Leaf Extract, *CO Pyrus Malus (Apple) Fruit Extract, *CO Spirulina Platensis Extract, Xanthan Gum.

*CO Certified Organic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EnglishAntibacterialHandSoap.jpgEnglishAntibacterialHandSoap.jpg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130817215004293GTIN-13: 0817215004293
EAN-13: 0817215004293
GTIN-12: 817215004293
UPC-A: 817215004293
GTIN storage (14 digits): 00817215004293
EnglishAntibacterialHandSoap.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68062-2242-12025-01-30C16284748780-12cef2736-a4df-d83d-e063-dadaa90ab31fDr Lift Antibacterial Hand Wash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68062-2242-1Dr Lift Antibacterial Hand Wash240 mg in 1 TUBEGEL2402

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68062-224268062-2242-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
Dr Lift Antibacterial Hand WashBENZALKONIUM CHLORIDESpa de Soleilab9e2c3c-d422-255e-e053-2a95a90a7a222026-04-30WarningsExact identifier
ndc (package): 68062-2242-1
ndc (product): 68062-2242
ndc11 (package): 68062224201
spl id: 50b719c9-4516-85fd-e063-6294a90a9103
spl set id: ab9e2c3c-d422-255e-e053-2a95a90a7a22

Reported adverse events (FAERS/openFDA)#

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