Aruba Sun SPF 70 Lotion

Manufacturer: Derma Care Research Labs, LLC | Derma Care Research Labs
Effective date: 2023-11-08
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:59:37

Label at a glance#

ProductAruba Sun SPF 70 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

LabelLabelLabelLabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72839-915-08	Aruba Sun SPF 70 Sunscreen	227 g in 1 BOTTLE, PLASTIC	LOTION	227	2
72839-915-18	Aruba Sun SPF 70 Sunscreen	227 g in 1 BOTTLE, PLASTIC	LOTION	227	2
72839-915-28	Aruba Sun SPF 70 Sunscreen	227 g in 1 BOTTLE, PLASTIC	LOTION	227	2
72839-915-38	Aruba Sun SPF 70 Sunscreen	227 g in 1 BOTTLE, PLASTIC	LOTION	227	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72839-915	ARUBA SUN SPF 70 SUNSCREEN (AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%) LOTION [DERMA CARE RESEARCH LABS, LLC]	2	Current NDC, Legacy NDC, 4 package rows	20231109_d96b4233-6d52-7621-e053-2a95a90a1b60.zip

Products#

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

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

Aruba Sun SPF 70 Sunscreen
Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%
TROLAMINE
EDETATE DISODIUM
OCTISALATE
EICOSYL POVIDONE
AVOBENZONE
OCTOCRYLENE
ALUMINUM STARCH OCTENYLSUCCINATE
TOCOPHEROL
BENZYL ALCOHOL
HOMOSALATE
ETHYLHEXYLGLYCERIN
PHENOXYETHANOL
POLYGLYCERYL-3 DISTEARATE
SORBITAN ISOSTEARATE
SORBITOL
STEARIC ACID
WATER
DIMETHICONE 350
CARBOMER 940

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72839-915	72839-915-08, 72839-915-28, 72839-915-18, 72839-915-38

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
Name	UNII	Kind
TROLAMINE	9O3K93S3TK	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
OCTISALATE	4X49Y0596W	ACTIB
EICOSYL POVIDONE	XQQ9MKE2BJ	IACT
AVOBENZONE	G63QQF2NOX	ACTIB
OCTOCRYLENE	5A68WGF6WM	ACTIB
ALUMINUM STARCH OCTENYLSUCCINATE	I9PJ0O6294	IACT
TOCOPHEROL	R0ZB2556P8	IACT
BENZYL ALCOHOL	LKG8494WBH	IACT
HOMOSALATE	V06SV4M95S	ACTIB
ETHYLHEXYLGLYCERIN	147D247K3P	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
POLYGLYCERYL-3 DISTEARATE	ZI1LK470XV	IACT
SORBITAN ISOSTEARATE	01S2G2C1E4	IACT
SORBITOL	506T60A25R	IACT
STEARIC ACID	4ELV7Z65AP	IACT
WATER	059QF0KO0R	IACT
DIMETHICONE 350	2Y53S6ATLU	IACT
CARBOMER 940	4Q93RCW27E	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aruba Sun SPF 70 Sunscreen	AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%	Derma Care Research Labs, LLC	d96b4233-6d52-7621-e053-2a95a90a1b60	2023-11-08	Warnings	Exact identifier ndc (package): 72839-915-18 ndc (package): 72839-915-08 ndc (package): 72839-915-28 ndc (package): 72839-915-38 ndc (product): 72839-915 ndc11 (package): 72839091518 ndc11 (package): 72839091538 ndc11 (package): 72839091528 ndc11 (package): 72839091508 spl id: 09ab318a-a6ca-eb9a-e063-6394a90ab602 spl set id: d96b4233-6d52-7621-e053-2a95a90a1b60

Reported adverse events (FAERS/openFDA)#

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