Aruba Sun SPF 50 Sunscreen

Product NDC: 72839-083
11-digit product format: 728390083
Labeler code: 72839
Product ID: 72839-083_29a4c95d-6cdf-955f-e063-6294a90a1846
Type: HUMAN OTC DRUG
Nonproprietary name: Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%
Dosage form: LOTION
Route: TOPICAL
Labeler: Derma Care Research Labs, LLC
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-11-25
Substance: OCTISALATE; AVOBENZONE; OCTOCRYLENE; HOMOSALATE
Active strength: 5; 3; 10; 15 g/100g; g/100g; g/100g; g/100g
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Aruba Sun SPF 50 Sunscreen
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTISALATE	5 g/100g
AVOBENZONE	3 g/100g
OCTOCRYLENE	10 g/100g
HOMOSALATE	15 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4X49Y0596W	Internal UNII lookup
G63QQF2NOX	Internal UNII lookup
5A68WGF6WM	Internal UNII lookup
V06SV4M95S	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
d8b28ce6-e938-c6e3-e053-2a95a90acc29	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72839-083-08	Aruba Sun SPF 50 Sunscreen	227 g in 1 BOTTLE, PLASTIC	LOTION	227	3
72839-083-18	Aruba Sun SPF 50 Sunscreen	227 g in 1 BOTTLE, PLASTIC	LOTION	227	3
72839-083-28	Aruba Sun SPF 50 Sunscreen	227 g in 1 BOTTLE, PLASTIC	LOTION	227	3
72839-083-38	Aruba Sun SPF 50 Sunscreen	227 g in 1 BOTTLE, PLASTIC	LOTION	227	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72839-083	ARUBA SUN SPF 50 SUNSCREEN (AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 10%) LOTION [DERMA CARE RESEARCH LABS, LLC]	3	Current NDC, Legacy NDC, 4 package rows	20241222_d8b28ce6-e938-c6e3-e053-2a95a90acc29.zip

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 92 of 353 · 7,049 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Royal Jelly Radiance Foundation Broad Spectrum SPF 20 Earth	OCTINOXATE, ZINC OXIDE	Distribuidora Comercial Jafra, S.A. de C.V.	0edc7bd4-9350-48e1-bbfe-e6450458ae59	2025-12-31	Warnings	Exact identifier application number: M020
Radiance Foundation Broad Spectrum SPF 20 - Bronze	OCTINOXATE, ZINC OXIDE	Distribuidora Comercial Jafra, S.A. de C.V.	90fbf555-106c-4131-b572-ead9bbb246e6	2025-12-31	Warnings	Exact identifier application number: M020
Radiance Foundation Broad Spectrum SPF 20 - Honey	OCTINOXATE, ZINC OXIDE	Distribuidora Comercial Jafra, S.A. de C.V.	1accbe67-c722-4af7-8422-0559ac4a987a	2025-12-31	Warnings	Exact identifier application number: M020
Radiance Foundation Broad Spectrum SPF 20 - Bare	OCTINOXATE, ZINC OXIDE	Distribuidora Comercial Jafra, S.A. de C.V.	5c0805c7-9b92-4c08-877c-64e720308430	2025-12-31	Warnings	Exact identifier application number: M020
Radiance Foundation Broad Spectrum SPF 20- Natural	OCTINOXATE, ZINC OXIDE	Distribuidora Comercial Jafra, S.A. de C.V.	0cc5429d-ace4-4060-b993-1b607218eaf8	2025-12-31	Warnings	Exact identifier application number: M020
Radiance Foundation Broad Spectrum SPF 20-Nude	OCTINOXATE, ZINC OXIDE	Distribuidora Comercial Jafra, S.A. de C.V.	b1851c5d-32ad-482a-bd24-2f280a68ef9e	2025-12-31	Warnings	Exact identifier application number: M020
Radiance Foundation Broad Spectrum SPF 20 -Spice	OCTINOXATE, ZINC OXIDE	Distribuidora Comercial Jafra, S.A. de C.V.	6164dc23-81c2-48b8-b309-2c5a81fe13a4	2025-12-31	Warnings	Exact identifier application number: M020
Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Light Medium	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	Pur-lisse Beauty, LLC	4744e501-f12a-6d25-e063-6394a90a2574	2025-12-31	Warnings	Exact identifier application number: M020
Radiance Foundation Broad Spectrum SPF 20 - Tawny	OCTINOXATE, ZINC OXIDE	Distribuidora Comercial Jafra, S.A. de C.V.	d7c4e758-3af2-40c6-bbe1-37e6fd0a5eb6	2025-12-31	Warnings	Exact identifier application number: M020
Radiance Foundation Broad Spectrum SPF 20 - Cappuccino	OCTINOXATE, ZINC OXIDE	Distribuidora Comercial Jafra, S.A. de C.V.	30601a73-089e-4fa7-8fb7-6b108498934a	2025-12-31	Warnings	Exact identifier application number: M020
Good Karma Dry Oil Mineral Sunscreen SPF-30	ZINC OXIDE SUNSCREEN	SOLARA SUNCARE, INC.	209c4913-29e6-24ca-e063-6294a90a6872	2025-12-31	Warnings	Exact identifier application number: M020
Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Medium	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	Pur-lisse Beauty, LLC	47456bf5-9f6c-e6a5-e063-6294a90a7054	2025-12-31	Warnings	Exact identifier application number: M020
Olay Age Defying Classic Daily Renewal Broad Spectrum SPF 15	OCTINOXATE AND ZINC OXIDE	The Procter & Gamble Manufacturing Company	60183a47-fd02-052b-e053-2991aa0a1b5c	2025-12-31	Warnings	Exact identifier application number: M020
Native Mineral Sunscreen Broad Spectrum SPF 30 Sweet Peach and Nectar	ZINC OXIDE	The Procter & Gamble Manufacturing Company	026dcaee-d33c-b874-e063-6394a90ad2e7	2025-12-31	Warnings	Exact identifier application number: M020
Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Tan	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	Pur-lisse Beauty, LLC	4745ab56-abaa-42de-e063-6394a90a6310	2025-12-31	Warnings	Exact identifier application number: M020
Olay Complete Plus Daily Facial Moisturizer with Sunscreen Broad Spectrum SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	The Procter & Gamble Manufacturing Company	22f645cf-5182-9e3f-e063-6394a90adc84	2025-12-31	Warnings	Exact identifier application number: M020
Native Mineral Sunscreen Broad Spectrum SPF 30 Tropical Breeze	ZINC OXIDE	The Procter & Gamble Manufacturing Company	232032b7-803f-40ec-e063-6394a90a4b38	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Sport Sunscreen SPF 100	AVOBENZONE 3%, HOMOSALATE 15%, OCTINOXATE 2% OCTISALATE 5%, OCTOCRYLENE 10%, OXYBENZONE 6%	Beiersdorf Inc	e1a9a831-a0b9-17ba-e053-2a95a90a3fa7	2025-12-31	Warnings	Exact identifier application number: M020
Radiant Glow Illuminating BB Cream Sunscreen SPF 30 - Tan Deep	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	Pur-lisse Beauty, LLC	4745ebec-acb0-77c4-e063-6394a90aee07	2025-12-31	Warnings	Exact identifier application number: M020
Coppertone Pure and Simple Baby Sunscreen SPF 50	ZINC OXIDE 24.08%	Beiersdorf Inc	08134b95-1879-27e5-e063-6294a90a29af	2025-12-31	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72839-083-08	72839008308	227 g in 1 BOTTLE, PLASTIC (72839-083-08)	227 g	2021-11-25	0000-00-00	No	No	Current
72839-083-18	72839008318	227 g in 1 BOTTLE, PLASTIC (72839-083-18)	227 g	2021-11-25		No	No	Current
72839-083-28	72839008328	227 g in 1 BOTTLE, PLASTIC (72839-083-28)	227 g	2021-11-25		No	No	Current
72839-083-38	72839008338	227 g in 1 BOTTLE, PLASTIC (72839-083-38)	227 g	2021-11-25		No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Aruba Sun SPF 50 Lotion	Derma Care Research Labs, LLC \| Derma Care Research Labs	2024-12-19	HUMAN OTC DRUG LABEL	3