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United States · US · US:53675-100_4a04fed7-e3c1-dc1e-e063-6294a90a2076
ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerARUBA ALOE BALM NV
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1153675100011 JAR in 1 BOX (53675-100-01) / 118 mL in 1 JAR
Annotations
UNII (FDA Substance ID)
4Y5P7MUD51
OCTINOXATE
RxCUI 13369
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4Y5P7MUD51",
"rxcui": "13369",
"inchikey": "YBGZDTIWKVFICR-JLHYYAGUSA-N",
"display_name": "OCTINOXATE",
"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": "53675-100_4a04fed7-e3c1-dc1e-e063-6294a90a2076",
"productndc": "53675-100",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; OXYBENZONE",
"proprietary_name": "ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE",
"active_ingred_unit": "mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "OCTINOXATE, OXYBENZONE",
"start_marketing_date": "20101101",
"active_numerator_strength": "75; 45"
}Related drugs
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