Label: DR LIFT SUN CARE SPF 25- titanium dioxide, zinc oxide lotion
- NDC Code(s): 68062-8821-1
- Packager: Spa de Soleil
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated March 21, 2023
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- Active Ingredients
- Purpose
- Warnings
- Directions
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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
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- INDICATIONS & USAGE
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INGREDIENTS AND APPEARANCE
DR LIFT SUN CARE SPF 25
titanium dioxide, zinc oxide lotionProduct 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)