🇺🇸
United States · US · US:72839-083_29a4c95d-6cdf-955f-e063-6294a90a1846
Aruba Sun SPF 50 Sunscreen
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDerma Care Research Labs, LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc117283908308227 g in 1 BOTTLE, PLASTIC (72839-083-08)
- ndc117283908318227 g in 1 BOTTLE, PLASTIC (72839-083-18)
- ndc117283908328227 g in 1 BOTTLE, PLASTIC (72839-083-28)
- ndc117283908338227 g in 1 BOTTLE, PLASTIC (72839-083-38)
Annotations
UNII (FDA Substance ID)
G63QQF2NOX
AVOBENZONE
RxCUI 45045
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "G63QQF2NOX",
"rxcui": "45045",
"inchikey": "XNEFYCZVKIDDMS-UHFFFAOYSA-N",
"display_name": "AVOBENZONE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"ad218ca8-103d-4cbe-b13d-6666c7d08d66": {
"match": "brand_token",
"title": "ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE (OCTINOXATE, OXYBENZONE) CREAM [ARUBA ALOE BALM NV]",
"spl_version": "3",
"published_date": "2026-02-16"
}
},
"productid": "72839-083_29a4c95d-6cdf-955f-e063-6294a90a1846",
"productndc": "72839-083",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "Aruba Sun SPF 50 Sunscreen",
"active_ingred_unit": "g/100g; g/100g; g/100g; g/100g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Avobenzone 3%, Homosalate 15%, Octisalate 5%, Octocrylene 10%",
"start_marketing_date": "20211125",
"active_numerator_strength": "3; 15; 5; 10"
}Access this data programmatically
Query Aruba Sun SPF 50 Sunscreen and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.