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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Dr Lift Sun Care SPF 25

Active Ingredients

Avobenzone 3.0%

Homosalate 15.0%

Octisalatae 5.0%

Purpose

Sunscreen

Warnings

Warnings

When using this product

Stop use and ask a doctor if

Keep out of reach of children

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

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

DrLiftSPF25_PRINT3aBOX

DR LIFT SUN CARE SPF 25 
titanium dioxide, zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68062-8821
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE2.25 mg  in 45 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1.35 mg  in 45 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE6.75 mg  in 45 mL
Inactive Ingredients
Ingredient NameStrength
ARGANIA SPINOSA SEED (UNII: 8H7X7XB54H)  
GLYCERIN (UNII: PDC6A3C0OX)  
CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)  
ALCOHOL (UNII: 3K9958V90M)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68062-8821-125 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/21/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM02003/21/2023
Labeler - Spa de Soleil (874682867)
Establishment
NameAddressID/FEIBusiness Operations
Spa de Soleil874682867manufacture(68062-8821)

Revised: 3/2023
Document Id: f76e616c-e11a-b509-e053-6294a90a2508
Set id: f76e616c-e119-b509-e053-6294a90a2508
Version: 1
Effective Time: 20230321
 
Spa de Soleil