Aloe Socotrina

UNIISPL

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

Identification

ManufacturerHahnemann Laboratories, INC.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
3766235401
200 PELLET in 1 VIAL, GLASS (37662-3540-1)
ndc11
3766235402
500 PELLET in 1 VIAL, GLASS (37662-3540-2)
ndc11
3766235403
3000 PELLET in 1 BOTTLE, GLASS (37662-3540-3)
ndc11
3766235404
10000 PELLET in 1 BOTTLE, GLASS (37662-3540-4)

Annotations

UNII (FDA Substance ID)

V5VD430YW9

ALOE

RxCUI 91263

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "V5VD430YW9",
    "rxcui": "91263",
    "inchikey": null,
    "display_name": "ALOE",
    "substance_type": "mixture",
    "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": "37662-3540_ffdb39ca-51a7-2267-e053-6394a90adf3f",
  "productndc": "37662-3540",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALOE",
  "proprietary_name": "Aloe Socotrina",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Aloe Socotrina",
  "start_marketing_date": "20230706",
  "active_numerator_strength": "200"
}

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