Anacardium Occidentale

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
6354596801
200 PELLET in 1 VIAL (63545-968-01)
ndc11
6354596802
500 PELLET in 1 VIAL (63545-968-02)
ndc11
6354596803
3000 PELLET in 1 BOTTLE, GLASS (63545-968-03)
ndc11
6354596804
10000 PELLET in 1 BOTTLE, GLASS (63545-968-04)

Annotations

UNII (FDA Substance ID)

4A10JR4E7E

ANACARDIUM OCCIDENTALE FRUIT

RxCUI 1358956

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "4A10JR4E7E",
    "rxcui": "1358956",
    "inchikey": null,
    "display_name": "ANACARDIUM OCCIDENTALE FRUIT",
    "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": "63545-968_2b4ac32a-66dd-9a05-e063-6294a90a1016",
  "productndc": "63545-968",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ANACARDIUM OCCIDENTALE FRUIT",
  "proprietary_name": "Anacardium Occidentale",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Anacardium Occidentale",
  "start_marketing_date": "20201102",
  "active_numerator_strength": "1"
}

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