Anacardium Orientale

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
6354597601
200 PELLET in 1 VIAL, GLASS (63545-976-01)
ndc11
6354597602
500 PELLET in 1 VIAL, GLASS (63545-976-02)
ndc11
6354597603
3000 PELLET in 1 BOTTLE, GLASS (63545-976-03)
ndc11
6354597604
10000 PELLET in 1 BOTTLE, GLASS (63545-976-04)

Annotations

UNII (FDA Substance ID)

Y0F0BU8RDU

SEMECARPUS ANACARDIUM JUICE

RxCUI 1350214

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "Y0F0BU8RDU",
    "rxcui": "1350214",
    "inchikey": null,
    "display_name": "SEMECARPUS ANACARDIUM JUICE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "98b62390-c29a-422e-98f9-ae1899fdcab6": {
      "match": "brand_token",
      "title": "ANACARDIUM COMBINATION 9205 (ANACARDIUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "63545-976_2b4ab488-302f-9255-e063-6294a90aa870",
  "productndc": "63545-976",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SEMECARPUS ANACARDIUM JUICE",
  "proprietary_name": "Anacardium Orientale",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Anacardium Orientale",
  "start_marketing_date": "20201110",
  "active_numerator_strength": "500"
}

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