FDA.reportPublic FDA data

Sand Sky Australian Sunshield Body Sunscreen SPF50 plus

Manufacturer
Supernova USA Inc. | Baxter Laboratories Pty. Ltd.
Effective date
2022-11-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:52:55

Label at a glance#

ProductSand Sky Australian Sunshield Body Sunscreen SPF50 plus
Active ingredientHOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
Label structure12 sections

Storage and handling

Other information Protect the product from excessive heat and direct sun Questions? Contact (626) 616-5811

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active Ingredients
Homosalate 10%
Octocrylene 8%
Octisalate 5%
Avobenzone 3%		Purpose
Sunscreen
Sunscreen
Sunscreen
Sunscreen

INDICATIONS & USAGE SECTION

Uses

  • Helps prevent sunburn.
  • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS SECTION

Warnings

For external use only.

Store below 30°C / 86°F and avoid direct sunlight.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. When using this product keep out of eyes. Rinse with water to remove.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply an even layer of this lotion on skin 20 minutes before sun exposure.
  • Reapply frequently especially after swimming, swaeting, or towelling.
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad-spectrum SPF of 15 or higher and other sun protection measures including:
    • Limit time in the sun, especially from 10 a.m. - 2. p.m.
    • Wear a long-sleeve shirts, pants, hats, and sunglasses.
  • Children under 6 months: ask a doctor.

INACTIVE INGREDIENT SECTION

Inactive ingredients Water (Aqua), Bees Wax, Aloe Barbadensis Leaf Juice, Isopropyl Palmitate, Cetearyl Alcohol, Cyclopentasiloxane, Cyclohexasiloxane, Ceteareth-20, Terminalia Ferdinandiana Fruit Extract, Glycerin, Sodium Stearoyl Glutamate, Tocopheryl Acetate, Carbomer, Hydroxyacetophenone, Benzyl Alcohol, Phenoxyethanol, Triethanolamine, Citric Acid.

STORAGE AND HANDLING SECTION

Other information

Protect the product from excessive heat and direct sun

Questions? Contact (626) 616-5811

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SAND
& SKY

Australian
Sunshield

Body Sunscreen SPF50+
Lotion Solaire Corporelle SPF50+

UVA + UVB
Board Spectrum SPF50+
80 Minutes Water Resistant
Lightweight

Net 190 mL / 6.42 fl. oz. US

SAND & SKY
SAND & SKY

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SAND
& SKY

Australian
Sunshield

Body Sunscreen SPF50+
Lotion Solaire Corporelle SPF50+

+ Vitamin E
+ Aloe Vera

UVA + UVB
Board Spectrum SPF50+
80 Minutes Water Resistant
Lightweight

Net 190 mL / 6.42 fl. oz. US

SAND & SKY
SAND & SKY

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82931-004-192025-01-30C16284748780-12cef2736-90ce-d83d-e063-dadaa90ab31fSAND & SKY AUSTRALIAN SUNSHIELD BODY SUNSCREEN SPF50+

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82931-004-19Sand Sky Australian Sunshield Body Sunscreen SPF50 plus1 in 1 CARTONLOTION11
82931-004-19Sand Sky Australian Sunshield Body Sunscreen SPF50 plus190 mL in 1 BOTTLE, PLASTICLOTION1901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82931-004SAND SKY AUSTRALIAN SUNSHIELD BODY SUNSCREEN SPF50 PLUS LOTION [SUPERNOVA USA INC.]1Legacy NDC, 2 package rows20230105_1ed8e7d6-4fa4-4725-9aa5-5861027a537e.zip

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
82931-00482931-004-19

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
HOMOSALATEV06SV4M95SACTIB
OCTOCRYLENE5A68WGF6WMACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB
WATER059QF0KO0RIACT
YELLOW WAX2ZA36H0S2VIACT
ALOE VERA LEAFZY81Z83H0XIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CYCLOMETHICONE 50THT5PCI0RIACT
CYCLOMETHICONE 6XHK3U310BAIACT
POLYOXYL 20 CETOSTEARYL ETHERYRC528SWUYIACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
BENZYL ALCOHOLLKG8494WBHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM STEAROYL GLUTAMATE65A9F4P024IACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT
KAKADU PLUM0ZQ1D2FDLIIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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
16e5b75e-6282-4df4-8f63-4a60bea58b851ed8e7d6-4fa4-4725-9aa5-5861027a537e2022-11-01WarningsExact identifier
spl id: 16e5b75e-6282-4df4-8f63-4a60bea58b85
spl set id: 1ed8e7d6-4fa4-4725-9aa5-5861027a537e

Reported adverse events (FAERS/openFDA)#

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