Solar Swipe Mineral Sunscreen SPF50

Manufacturer
Guangzhou Fantesy Biotechnology Co.,Ltd
Effective date
2026-01-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:31:44

Label at a glance#

ProductSolar Swipe Mineral Sunscreen SPF50
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure12 sections

Indications and uses

1. Helps prevent sunburn 2. Provides broad-spectrum UVA/UVB protection 1. ldeal for daily use, especially in outdoor environments 2. Lightweight powder format helps reduce shine and sets makeup

Dosage and administration

·Apply evenly to clean, dry skin 15 minutes before sun exposure ·Reapply every 2 hours or after sweating, swimming, or towel drying ·Use daily for best results

Storage and handling

Room temperature preservation

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 22%
Titanium Dioxide 2%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

1. Helps prevent sunburn
2. Provides broad-spectrum
UVA/UVB protection
1. ldeal for daily use, especially in outdoor environments
2. Lightweight powder format helps reduce shine and sets makeup

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

When using this product, keep out of eyes. Rinse with water to remove.

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if rash or irritation occurs.

Keep out of

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, seek medical help.

Directions

DOSAGE & ADMINISTRATION SECTION

·Apply evenly to clean, dry skin 15 minutes before sun exposure
·Reapply every 2 hours or after sweating, swimming, or towel drying
·Use daily for best results

Other information

STORAGE AND HANDLING SECTION

Room temperature preservation

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Water, Isohexadecane, Cyclopentasiloxane, Propylene Glycol, Silica Microspheres, Rubus
Idaeus (Raspberry) Seed Oil, Potassium Cetyl Phosphate, Lichen Extract, Ceramide NP, Dimethicone, Squalane,
Phytoplankton Extract, PEG-7 Glyceryl Cocoate, Polyhydroxystearic Acid, Sodium Hyaluronate, Glycerin,
Leuconostoc/Radish Root Ferment Filtrate, Butylene Glycol, Potassium Sorbate, CI 77492, CI 77491,
Mentholum, CI 77499

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130199284307933GTIN-13: 0199284307933
EAN-13: 0199284307933
GTIN-12: 199284307933
UPC-A: 199284307933
GTIN storage (14 digits): 00199284307933
label.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83447-015-01Solar Swipe Mineral Sunscreen SPF5050 g in 1 BOTTLECREAM501

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83447-01583447-015-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

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
Solar Swipe Mineral Sunscreen SPF50SOLAR SWIPE MINERAL SUNSCREEN SPF50Guangzhou Fantesy Biotechnology Co.,Ltd47d75d61-5295-3eab-e063-6394a90a01c12026-01-07WarningsExact identifier
ndc (package): 83447-015-01
ndc (product): 83447-015
ndc11 (package): 83447001501
spl id: 47d7636d-a0b4-f0b6-e063-6294a90ae469
spl set id: 47d75d61-5295-3eab-e063-6394a90a01c1

Reported adverse events (FAERS/openFDA)#

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