FDA.reportPublic FDA data

Dr Lift SPF 50 Mineral Sunscreen Stick

Manufacturer
Spa de Soleil
Effective date
2025-11-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:26:47

Label at a glance#

ProductDr Lift SPF 50 Mineral Sunscreen Stick
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 25%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Warnings

WARNINGS SECTION

Warnings:

For external use only. 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 right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions: Apply generously and evenly 15 minutes before sun exposure. Ensure complete coverage to the area above the lip, nose, and tops of ears.

INDICATIONS & USAGE SECTION

Uses
Provides high protection against sunburn.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Caprylic/Capric Triglyceride, Helianthus Annuus (Sunflower) Seed Oil, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Butyrospermum Parkii (Shea) Butter, Cetyl Alcohol, Euphorbia Cerifera (Candelilla) Wax, Helianthus Annuus (Sunflower) Seed Wax, Microcrystalline cellulose, Cocos Nucifera (Coconut) Oil, **Squalane, Tocopheryl Acetate (Vitamin E), Benzyl Alcohol.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DrLift Mineral Stick SPF 50DrLift Mineral Stick SPF 50

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68062-8314-1Dr Lift SPF 50 Mineral Sunscreen Stick15 g in 1 TUBESTICK151

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68062-831468062-8314-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
HELIANTHUS ANNUUS SEED WAX42DG15CHXVIACT
PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL66YXD4DKO9IACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT
CETYL ALCOHOL936JST6JCNIACT
EUPHORBIA CERIFERA (CANDELILLA) WAXWL0328HX19IACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLEST7ZE2WA4MBIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
COCOS NUCIFERA (COCONUT) OILQ9L0O73W7LIACT
SQUALANEGW89575KF9IACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
ZINC OXIDESOI2LOH54ZACTIB
BENZYL ALCOHOLLKG8494WBHIACT

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 SPF 50 Mineral Sunscreen StickZINC OXIDESpa de Soleil436fdf4f-11db-7c5b-e063-6294a90a87312025-11-12WarningsExact identifier
ndc (package): 68062-8314-1
ndc (product): 68062-8314
ndc11 (package): 68062831401
spl id: 436fdf4f-11da-7c5b-e063-6294a90a8731
spl set id: 436fdf4f-11db-7c5b-e063-6294a90a8731

Reported adverse events (FAERS/openFDA)#

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