DR LIFT ADVANCED ANTIBACTERIAL WIPES- benzalkonium chloride liquid

Dr Lift Advanced Antibacterial Wipes by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Warnings

Warnings

For external use only. Do not use if you are allergic to any of these ingredients. 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

Keep out of reach of children.

Directions

Take wipe and rub thoroughly over all surfaces of both hands. Rub hands together briskly to dry and allow to air dry. Dispose of wipe in trash. Do not flush.

To Dispense: Peel back front label slowly. Remove Wipes.

To Reseal: Firmly run thumb over the label. Dispose of wipe in trash. Do not flush.

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, Decyl Glucoside, Glycerin, *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, Potassium Sorbate, Sodium Benzoate. *CO Certified Organic

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR LIFT ADVANCED ANTIBACTERIAL WIPES 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68062-2244
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.156 mg  in 120 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68062-2244-1	120 mg in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/17/2020

Labeler - Spa de Soleil (874682867)

Establishment
Name	Address	ID/FEI	Business Operations
Spa de Soleil		874682867	manufacture(68062-2244)