FDA.reportPublic FDA data

Bondi Sands Sport SPF 50 Sunscreen

Manufacturer
BONDI SANDS (USA) INC.
Effective date
2024-11-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:35:12

Label at a glance#

ProductBondi Sands Sport SPF 50 Sunscreen
Active ingredientAVOBENZONE, OCTISALATE, OCTOCRYLENE, HOMOSALATE
Label structure10 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. Retains SPF after 80 minutes of activity in the water.

Dosage and administration

Apply liberally 15 minutes before sun exposure. Reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 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 a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in ...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%

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.
  • Retains SPF after 80 minutes of activity in the water.

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

OTC - STOP USE SECTION

if 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 15 minutes before sun exposure.
  • Reapply:
  • after 80 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 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 a Broad Spectrum SPF value 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 sleeved shirts, pants, hats, and sunglasses.
  • Children under 6 months: Ask a doctor.

Other information

OTHER SAFETY INFORMATION

  • Protect the product in this container from excessive heat and direct sun.
  • You may report a serious adverse reaction to 888-266-0772; Monday – Friday, 9 am – 5 pm.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water/Aqua/Eau, Beeswax/Cera Alba/Cire d'abeille, C12-15 Alkyl Benzoate, Cetyl Dimethicone, Cocoglycerides, PEG-15 Cocamine, Glycerin, PEG-40 Stearate, Phenoxyethanol, Saccharide Isomerate, Caprylyl Glycol, Disodium EDTA, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Caprylhydroxamic Acid, Tocopheryl Acetate, Aloe Barbadensis Extract, Citric Acid, Sodium Citrate, Potassium Sorbate, Sodium Benzoate.

Questions?

OTC - QUESTIONS SECTION

888-266-0772 or visit bondisands.com

Company Information

SPL UNCLASSIFIED SECTION

Made in Australia.

Distributed by Bondi Sands USA

Wilmington, 19808, DE.

bondisands.com

Product Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sport triggersport trigger

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79950-015-01Bondi Sands Sport SPF 50 Sunscreen300 mL in 1 BOTTLE, SPRAYLOTION3002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79950-015BONDI SANDS SPORT SPF 50 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [BONDI SANDS (USA) INC.]2Legacy NDC, 1 package rows20241108_e99d806f-a869-77c0-e053-2995a90ab99c.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79950-01579950-015-01

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
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM CITRATE1Q73Q2JULRIACT
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
YELLOW WAX2ZA36H0S2VIACT
PEG-15 COCAMINE8L6LB12TSJIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SACCHARIDE ISOMERATEW8K377W98IIACT
CAPRYLYL GLYCOL00YIU5438UIACT
COCO-GLYCERIDESISE9I7DNUGIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT
EDETATE DISODIUM7FLD91C86KIACT
TROLAMINE9O3K93S3TKIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
ALOE VERA WHOLEKIZ4X2EHYXIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
OCTOCRYLENE5A68WGF6WMACTIB
PEG-40 STEARATEECU18C66Q7IACT
HOMOSALATEV06SV4M95SACTIB
WATER059QF0KO0RIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
CETYL DIMETHICONE 45IK315POC44IACT
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)809Y72KV36IACT

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
26438236-13b8-c0c0-e063-6394a90a952de99d806f-a869-77c0-e053-2995a90ab99c2024-11-06WarningsExact identifier
spl id: 26438236-13b8-c0c0-e063-6394a90a952d
spl set id: e99d806f-a869-77c0-e053-2995a90ab99c

Reported adverse events (FAERS/openFDA)#

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