Dr Lift Unscented Antibacterial Body Wash

Manufacturer
Spa de Soleil
Effective date
2026-01-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:53:14

Label at a glance#

ProductDr Lift Unscented Antibacterial Body Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Directions: Wet your skin in the shower or bath. Lather body wash on your hands and use a loofah or a washcloth to apply it to your skin. Rinse it off and pat dry with a towel. 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. If product gets in eyes, rinse promptly and thoroughly with water. Discontinue use if irritation and redness occur. Stop use and ask a doctor if irritation or redness lasts for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

INDICATIONS & USAGE SECTION

Directions: Wet your skin in the shower or bath. Lather body wash on your hands and use a loofah or a washcloth to apply it to your skin. Rinse it off and pat dry with a towel.

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:

Aqua, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Glycerin, Guar Hydroxypropyltrimonium Chloride, Sodium Chloride, *CO 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, Citric Acid, Dehydroacetic Acid, Benzyl Alcohol.

*CO Certified Organic

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DLABW104-UNS-8.jpgDLABW104-UNS-8.jpg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130817215005528GTIN-13: 0817215005528
EAN-13: 0817215005528
GTIN-12: 817215005528
UPC-A: 817215005528
GTIN storage (14 digits): 00817215005528
DLABW104-UNS-8.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68062-2248-12026-01-22C16284748780-12cef2736-a4ee-d83d-e063-dadaa90ab31fDr Lift Unscented Antibacterial Body Wash
68062-2248-12025-01-30C16284748780-12cef2736-a4ee-d83d-e063-dadaa90ab31fDr Lift Unscented Antibacterial Body Wash

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68062-224868062-2248-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
50b66230-f8b3-f45c-e063-6394a90aeda7da472f3a-6a7f-6a81-e053-2a95a90a12062026-04-30WarningsExact identifier
spl set id: da472f3a-6a7f-6a81-e053-2a95a90a1206

Reported adverse events (FAERS/openFDA)#

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