Aruba Aloe Lip Sunscreen and Moisturizer

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerAruba Aloe Balm NV

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5367514001
4.8 g in 1 TUBE (53675-140-01)

Annotations

UNII (FDA Substance ID)

95OOS7VE0Y

OXYBENZONE

RxCUI 32673

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "95OOS7VE0Y",
    "rxcui": "32673",
    "inchikey": "DXGLGDHPHMLXJC-UHFFFAOYSA-N",
    "display_name": "OXYBENZONE",
    "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": "53675-140_09862169-501d-f8eb-e063-6294a90a6f2d",
  "productndc": "53675-140",
  "dosage_form": "LIPSTICK",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OXYBENZONE; PADIMATE O",
  "proprietary_name": "Aruba Aloe Lip Sunscreen and Moisturizer",
  "active_ingred_unit": "g/100g; g/100g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "OXYBENZONE, PADIMATE",
  "start_marketing_date": "20110601",
  "active_numerator_strength": "3; 8"
}

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