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United States · US · US:53675-157_0a21d8e0-059f-e088-e063-6394a90a2d1d

Aruba Aloe Very Water Resistant Sunscreen

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

  • ndc11
    5367515706
    177 mL in 1 BOTTLE (53675-157-06)

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": "53675-157_0a21d8e0-059f-e088-e063-6394a90a2d1d",
  "productndc": "53675-157",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTINOXATE; OXYBENZONE",
  "proprietary_name": "Aruba Aloe Very Water Resistant Sunscreen",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "OCTINOXATE, OXYBENZONE",
  "start_marketing_date": "20110708",
  "active_numerator_strength": "70; 20"
}

Related drugs

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