Aloe

UNIISPL

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

Identification

ManufacturerBoiron

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0220018941
5 [hp_C] in 1 TUBE (0220-0189-41)

Annotations

UNII (FDA Substance ID)

0D145J8EME

ALOE FEROX LEAF

RxCUI 1309503

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "0D145J8EME",
    "rxcui": "1309503",
    "inchikey": null,
    "display_name": "ALOE FEROX LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "860c9942-0699-40c9-be1e-67f54d7cdf4d": {
      "match": "brand_token",
      "title": "ALOE UP SPF 50 MINERAL (ZINC OXIDE, TITANIUM DIOXIDE) SPRAY [INSPEC SOLUTIONS, LLC]",
      "spl_version": "2",
      "published_date": "2026-05-11"
    }
  },
  "productid": "0220-0189_0051c7de-8a83-0905-e063-6294a90a0bec",
  "productndc": "0220-0189",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALOE FEROX LEAF",
  "proprietary_name": "Aloe",
  "active_ingred_unit": "[hp_C]/5[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "ALOE FEROX LEAF",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "5"
}

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