FDA.reportPublic FDA data

Aruba Sun SPF 50 Lotion

Manufacturer
Derma Care Research Labs, LLC | Derma Care Research Labs
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:47:57

Label at a glance#

ProductAruba Sun SPF 50 Sunscreen
Active ingredientOCTISALATE, AVOBENZONE, OCTOCRYLENE, HOMOSALATE
Label structure8 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 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 n the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measure including: limit time in the sun, especial...

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

DOSAGE & ADMINISTRATION 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 on damaged or broken skin. When using this product keep out of eyes. Rinse eyes with water to remove.

Stop use and ask a doctor 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

INDICATIONS & USAGE 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 n the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measure including:

  • limit time in the sun, especially from 10 am to 2 pm
  • wear long-sleeved shirts, pants, hats, and sunglasses.
  • Children under 6 months: ask a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aluminum Starch Octenylsuccinate, Benzyl Alcohol, Carbomer, Dimethicone, Disodium EDTA, Ethylhexylglycerin, Fragrance, Phenoxyethanol, Polyglyceryl-3 Distearate, Sorbitan Isostearate, Sorbitol, Stearic Acid, Tocopherol, Triethanolamine, VP/Eicosene Copolymer, Water

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabelLabelLabelLabelLabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72839-083-08Aruba Sun SPF 50 Sunscreen227 g in 1 BOTTLE, PLASTICLOTION2273
72839-083-18Aruba Sun SPF 50 Sunscreen227 g in 1 BOTTLE, PLASTICLOTION2273
72839-083-28Aruba Sun SPF 50 Sunscreen227 g in 1 BOTTLE, PLASTICLOTION2273
72839-083-38Aruba Sun SPF 50 Sunscreen227 g in 1 BOTTLE, PLASTICLOTION2273

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72839-083ARUBA SUN SPF 50 SUNSCREEN (AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%) LOTION [DERMA CARE RESEARCH LABS, LLC]3Current NDC, Legacy NDC, 4 package rows20241222_d8b28ce6-e938-c6e3-e053-2a95a90acc29.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72839-08372839-083-08, 72839-083-18, 72839-083-28, 72839-083-38

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
TROLAMINE9O3K93S3TKIACT
EDETATE DISODIUM7FLD91C86KIACT
OCTISALATE4X49Y0596WACTIB
EICOSYL POVIDONEXQQ9MKE2BJIACT
AVOBENZONEG63QQF2NOXACTIB
OCTOCRYLENE5A68WGF6WMACTIB
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
TOCOPHEROLR0ZB2556P8IACT
BENZYL ALCOHOLLKG8494WBHIACT
HOMOSALATEV06SV4M95SACTIB
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYGLYCERYL-3 DISTEARATEZI1LK470XVIACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
SORBITOL506T60A25RIACT
STEARIC ACID4ELV7Z65APIACT
WATER059QF0KO0RIACT
DIMETHICONE 3502Y53S6ATLUIACT
CARBOMER 9404Q93RCW27EIACT

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
Aruba Sun SPF 50 SunscreenAVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%Derma Care Research Labs, LLCd8b28ce6-e938-c6e3-e053-2a95a90acc292024-12-19WarningsExact identifier
ndc (package): 72839-083-08
ndc (package): 72839-083-18
ndc (package): 72839-083-28
ndc (package): 72839-083-38
ndc (product): 72839-083
ndc11 (package): 72839008318
ndc11 (package): 72839008308
ndc11 (package): 72839008338
ndc11 (package): 72839008328
spl id: 29a4c95d-6cdf-955f-e063-6294a90a1846
spl set id: d8b28ce6-e938-c6e3-e053-2a95a90acc29

Reported adverse events (FAERS/openFDA)#

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