Home NDC 72839-083 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.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength 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 26 of 357 · 7,139 matching rows.
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