DR LIFT SUN CARE SPF 25- titanium dioxide, zinc oxide lotion

Dr Lift Sun Care SPF 25 by

Drug Labeling and Warnings

Dr Lift Sun Care SPF 25 by is a Otc medication manufactured, distributed, or labeled by Spa de Soleil. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Avobenzone 3.0%

Homosalate 15.0%

Octisalatae 5.0%

Purpose

Sunscreen

Warnings

Warnings

• Do not use on damaged or broken skin

When using this product

• Keep out of eyes. Rinse with water to remove

Stop use and ask a doctor if

• rash occurs

Keep out of reach of children

• If swallowed, get medical help or contact a Poison Control Center immediately

Directions

Directions: for sunscreen use

. apply generously 15 minutes before sun exposure

. apply to all skin exposed to the sun

. children under 6 months of age: ask a doctor

Inactive Ingredients

Inactive Ingredients: Aqua, SD Alcohol 40-B, Glycerin, Argania Spinosa Kernel Oil, Cetearyl Ethylhexanoate, Ammonium Polyacryloyldimethyl Taurate, Bisabolol, *CO Glycerin, Tocopheryl Acetate (Vitamin E), *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, Phenoxyethanol, Ethylhexylglycerin.

*CO - Certified Organic

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

Directions: for sunscreen use

. apply generously 15 minutes before sun exposure

. apply to all skin exposed to the sun

. children under 6 months of age: ask a doctor

Other information

.protect the product in this container from excessive heat and direct sun

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR LIFT SUN CARE SPF 25 
titanium dioxide, zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68062-8821
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	2.25 mg  in 45 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	1.35 mg  in 45 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	6.75 mg  in 45 mL

Inactive Ingredients
Ingredient Name	Strength
ARGANIA SPINOSA SEED (UNII: 8H7X7XB54H)
GLYCERIN (UNII: PDC6A3C0OX)
CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68062-8821-1	25 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/21/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	M020	03/21/2023

Labeler - Spa de Soleil (874682867)

Establishment
Name	Address	ID/FEI	Business Operations
Spa de Soleil		874682867	manufacture(68062-8821)