FDA.reportPublic FDA data

Dr Lift Mineral SPF 50

Manufacturer
Spa de Soleil
Effective date
2025-10-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:38:29

Label at a glance#

ProductDr Lift Mineral SPF 50
Active ingredientTITANIUM DIOXIDE, ZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 7.2%

Zinc Oxide 9.52%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Warnings

WARNINGS SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

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 SECTION

Uses
Provides high protection against sunburn.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DeLift_Sprayspf50DeLift_Sprayspf50

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68062-8311-1Dr Lift Mineral SPF 50100 mL in 1 BOTTLE, SPRAYSPRAY1001

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68062-831168062-8311-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINALMI26O6933IACT
ORYZA SATIVA (RICE) BRANR60QEP13ICIACT
STEARIC ACID4ELV7Z65APIACT
SQUALANEGW89575KF9IACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
HELIANTHUS ANNUUS FLOWERING TOPBKJ0J3D1BPIACT
PONGAMIA GLABRA SEED OIL62160PU6FJIACT
ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL8LGU7VM393IACT
TOCOPHEROLR0ZB2556P8IACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
CARTHAMUS TINCTORIUS (SAFFLOWER) SEED OIL65UEH262ISIACT
COCONUT ALKANES1E5KJY107TIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
VITIS VINIFERA (GRAPE) SEED OIL930MLC8XGGIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
ZINC OXIDESOI2LOH54ZACTIB
OLEA EUROPAEA (OLIVE) FRUIT OIL6UYK2W1W1EIACT
ARGANIA SPINOSA KERNEL OIL4V59G5UW9XIACT
BISABOLOL24WE03BX2TIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dr Lift Mineral SPF 50TITANIUM DIOXIDE, ZINC OXIDESpa de Soleil40c03d65-8d09-371a-e063-6294a90a7ac62025-10-09WarningsExact identifier
ndc (package): 68062-8311-1
ndc (product): 68062-8311
ndc11 (package): 68062831101
spl id: 40c04b10-2eb5-3a52-e063-6394a90ad407
spl set id: 40c03d65-8d09-371a-e063-6294a90a7ac6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.