FDA.reportPublic FDA data

Pursuit Body Surf Daily SPF 40 Body Sunscreen

Manufacturer
Pursuit Beauty Inc. | Product Society LLC
Effective date
2022-12-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:52:20

Label at a glance#

ProductPursuit Body Surf Daily SPF 40 Body Sunscreen
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure9 sections

Indications and uses

helps prevent sunburn decreases the risk of skin cancer and early skin aging caused by the sun.

Dosage and administration

apply liberally 15 minutes before sun exposure children under 6 months of age: Ask a doctor reapply after 40 minutes of swimming or sweating, immediately after towel drying, at least every 2 hours

Storage and handling

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

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active IngredientsPurpose
Avobenzone (3.0%)Sunscreen
Homosalate (15.0%)Sunscreen
Octisalate (5.0%)Sunscreen
Octocrylene (10.0%)Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • decreases the risk of skin cancer and early skin aging caused by the sun.

Warnings

WARNINGS SECTION

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin

OTC - WHEN USING SECTION

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

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally 15 minutes before sun exposure
  • children under 6 months of age: Ask a doctor
  • reapply after 40 minutes of swimming or sweating, immediately after towel drying, at least every 2 hours

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Polysorbate 20, Cetearyl Alcohol, Glyceryl Stearate, Glycerin, Polysorbate 60, Polyester-7, Neopentyl Glycol Diheptanoate, VP/Hexadecene Copolymer, Aloe Barbadensis Leaf Juice, Carbomer, Xanthan Gum, Sodium Hydroxide, Tetrasodium Glutamate Diacetate, Phenoxyethanol, Ethylhexylglycerin.

Other Information

STORAGE AND HANDLING SECTION

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

SPL UNCLASSIFIED SECTION

Distributed by:
Pursuit Beauty Inc. with
offices at 3381 Robertson Place, Los Angeles, CA,
90034, USA.

PRINCIPAL DISPLAY PANEL - 90 mL Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BODY SURF

DAILY SPF 40
BODY SUNSCREEN

pursuit
CLEAN, ACTIVE, EFFORTLESS

3 fl oz / 90 mL

PRINCIPAL DISPLAY PANEL - 90 mL Tube Carton
PRINCIPAL DISPLAY PANEL - 90 mL Tube Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83040-001-012025-01-30C16284748780-12cef2736-af88-d83d-e063-dadaa90ab31fPursuit Body Surf Daily SPF 40 Body Sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83040-001-01Pursuit Body Surf Daily SPF 40 Body Sunscreen90 g in 1 TUBELOTION901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83040-001PURSUIT BODY SURF DAILY SPF 40 BODY SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [PURSUIT BEAUTY INC.]1Legacy NDC, 1 package rows20221209_94295ecb-1580-4135-bcab-3c0f599cfe6e.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83040-00183040-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
WATER059QF0KO0RIACT
POLYSORBATE 207T1F30V5YHIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
GLYCERINPDC6A3C0OXIACT
POLYSORBATE 60CAL22UVI4MIACT
POLYESTER-70841698D2FIACT
NEOPENTYL GLYCOL DIHEPTANOATE5LKW3C543XIACT
VINYLPYRROLIDONE/HEXADECENE COPOLYMERKFR5QEN0N9IACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
XANTHAN GUMTTV12P4NEEIACT
SODIUM HYDROXIDE55X04QC32IIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT

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
2e5eb337-081a-405b-8b3b-b30b36c35c3094295ecb-1580-4135-bcab-3c0f599cfe6e2022-12-02WarningsExact identifier
spl id: 2e5eb337-081a-405b-8b3b-b30b36c35c30
spl set id: 94295ecb-1580-4135-bcab-3c0f599cfe6e

Reported adverse events (FAERS/openFDA)#

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