DR LIFT MINERAL SPF 50- titanium dioxide, zinc oxide spray

Dr Lift Mineral SPF 50 by

Drug Labeling and Warnings

Dr Lift Mineral SPF 50 by is a Otc medication manufactured, distributed, or labeled by Spa de Soleil. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Titanium Dioxide 7.2%

Zinc Oxide 9.52%

Purpose

Sunscreen

Warnings

WarningsWhen using this product

• keep out of the eye area
• rinse with water to remove
• stop use and ask a doctor if rash or irritation develops
• for external use onlyl
• keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions

Shake before spraying. Spray into hands to apply to face. Apply thin layer over clean, dry skin. Massage well. Allow 15 minutes of complete penetration before sun exposure. Reapply every 1-2 hours & after swimming or sweating. Protect the product in this container from excessive heat.

INDICATIONS & USAGE

Uses
Provides high protection against sunburn.

Inactive Ingredients

Inactive Ingredients:

Carthamus Tinctorius (Safflower) Seed Oil, Coconut Alkanes (And) Coco-Caprylate/Caprate, Caprylic/Capric Triglyceride, Helianthus Annuus (Sunflower) Seed Oil, Vitis Vinifera (Grape) Seed Oil, *CO Pongamia Glabra Seed Oil, Olea Europaea (Olive) Fruit Oil, Argania Spinosa Kernel Oil, Stearic Acid, Polyhydroxystearic Acid, Tocopheryl Acetate (Vitamin E), Alumina, Oryza Sativa (Rice) Bran Extract, Bisabolol, Helianthus Annuus (Sunflower) Extract, **Squalane, Rosmarinus Officinalis (Rosemary) Leaf Extract, Tocopherol.

Principal Display Panel

INGREDIENTS AND APPEARANCE

DR LIFT MINERAL SPF 50 
titanium dioxide, zinc oxide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68062-8311
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	72 mg  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	952 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALUMINA (UNII: LMI26O6933)
ORYZA SATIVA (RICE) BRAN (UNII: R60QEP13IC)
STEARIC ACID (UNII: 4ELV7Z65AP)
SQUALANE (UNII: GW89575KF9)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
PONGAMIA GLABRA SEED OIL (UNII: 62160PU6FJ)
ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL (UNII: 8LGU7VM393)
TOCOPHEROL (UNII: R0ZB2556P8)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARTHAMUS TINCTORIUS (SAFFLOWER) SEED OIL (UNII: 65UEH262IS)
COCONUT ALKANES (UNII: 1E5KJY107T)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI)
VITIS VINIFERA (GRAPE) SEED OIL (UNII: 930MLC8XGG)
OLEA EUROPAEA (OLIVE) FRUIT OIL (UNII: 6UYK2W1W1E)
ARGANIA SPINOSA KERNEL OIL (UNII: 4V59G5UW9X)
BISABOLOL (UNII: 24WE03BX2T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68062-8311-1	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/09/2025

Labeler - Spa de Soleil (874682867)

Establishment
Name	Address	ID/FEI	Business Operations
Spa de Soleil		874682867	manufacture(68062-8311)