Dr Lift Unscented Antibacterial Body Wash

Dr Lift Unscented Antibacterial Body Wash by

Drug Labeling and Warnings

Dr Lift Unscented Antibacterial Body Wash by is a Otc medication manufactured, distributed, or labeled by Spa de Soleil. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DR LIFT UNSCENTED ANTIBACTERIAL BODY WASH- benzalkonium chloride liquid 
Spa de Soleil

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Dr Lift Unscented Antibacterial Body Wash

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Warnings

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.

Keep out of reach of children.

Directions

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:

Inactive Ingredients

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

DR LIFT UNSCENTED ANTIBACTERIAL BODY WASH 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68062-2248
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.312 mg  in 240 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68062-2248-1	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/15/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/15/2022	04/30/2026

Labeler - Spa de Soleil (874682867)

Establishment
Name	Address	ID/FEI	Business Operations
Spa de Soleil		874682867	manufacture(68062-2248)

Revised: 4/2026

Document Id: 50b66230-f8b3-f45c-e063-6394a90aeda7

34390-5

Set id: da472f3a-6a7f-6a81-e053-2a95a90a1206

Version: 3

Effective Time: 20260430