FDA.reportPublic FDA data

Sunski Base Camp Face & Body Sunscreen SPF 45

Manufacturer
Stewart Charley Ventures, LLC
Effective date
2026-08-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-09-03 03:03:53

Label at a glance#

ProductSunski Base Camp Face and Body Sunscreen SPF 45
Active ingredientHOMOSALATE, OCTISALATE, AVOBENZONE
Label structure9 sections

Indications and 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.

Dosage and administration

Apply liberally and evenly 15 minutes before sun exposure. Reapply: After 40 minutes of swimming or sweating Immediately after towel drying At least every two hours 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 Broad Spectrum SPF of 15 or higher and other sun protection measures including: Limit time ...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Homosalate 15%
Octisalate 5%
Avobenzone 3%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

• 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

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally and evenly 15 minutes before sun exposure. Reapply:
  • After 40 minutes of swimming or sweating
  • Immediately after towel drying
  • At least every two hours
  • 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 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 long-sleeve shirts, pants, hats, and sunglasses

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Butyloctyl Salicylate, Glycerin, Butylene Glycol, Polyglyceryl-3 Distearate, Polyglyceryl-6 Stearate, Cetearyl Alcohol, Benotriazolyl Dodecyl p-Cresol, Jojoba Esters, Polymethylsilsesquioxane, Poly C10-30 Alkyl Acrylate, 1,2-Hexanediol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, Glyceryl Stearate Citrate, Fragrance, Caprylyl Glycol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Phospholipids, Polyglyceryl-6 Behenate, Allantoin, Ethylhexylglycerin, Xanthan Gum, Tocopherol

Other Information

SPL UNCLASSIFIED SECTION

Protect the product in this container from excessive heat and direct sun

Questions or Comments?

OTC - QUESTIONS SECTION

Contact: hello@sunski.com

Package Labeling:75mL- 87626-001-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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labellabel

Package Labeling:150mL-87626-001-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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labellabel

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87626-00187626-001-00, 87626-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB
WATER059QF0KO0RIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
GLYCERINPDC6A3C0OXIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
POLYGLYCERYL-3 DISTEARATEZI1LK470XVIACT
POLYGLYCERYL-6 STEARATEETY9Q81E2TIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
BENZOTRIAZOLYL DODECYL P-CRESOL298PX4M11XIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
TROMETHAMINE023C2WHX2VIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
CAPRYLYL GLYCOL00YIU5438UIACT
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMERW59H9296ZGIACT
POLYGLYCERYL-6 BEHENATE4T2L7QI313IACT
ALLANTOIN344S277G0ZIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
XANTHAN GUMTTV12P4NEEIACT
TOCOPHEROLR0ZB2556P8IACT
JOJOBA OIL, RANDOMIZED7F0EV20QYLIACT
POLYMETHYLSILSESQUIOXANE/TRIMETHYLSILOXYSILICATEX2PZH4Y6HTIACT
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
BEHENYL ACRYLATE POLYMERD64PM5UT4UIACT

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
Sunski Base Camp Face and Body Sunscreen SPF 45HOMOSALATE, OCTISALATE, AVOBENZONEStewart Charley Ventures, LLC2fc45f85-a6f8-4893-8b34-4db5e39cb6152026-08-20WarningsExact identifier
ndc (package): 87626-001-00
ndc (package): 87626-001-01
ndc (product): 87626-001
ndc11 (package): 87626000100
ndc11 (package): 87626000101
spl id: 597c115b-ceb8-9313-e063-6394a90a0228
spl set id: 2fc45f85-a6f8-4893-8b34-4db5e39cb615

Reported adverse events (FAERS/openFDA)#

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