Lycopodium Clavatum

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
3766217831
200 PELLET in 1 VIAL, GLASS (37662-1783-1)
ndc11
3766217832
500 PELLET in 1 VIAL, GLASS (37662-1783-2)
ndc11
3766217833
3000 PELLET in 1 BOTTLE, GLASS (37662-1783-3)
ndc11
3766217834
10000 PELLET in 1 BOTTLE, GLASS (37662-1783-4)

Annotations

UNII (FDA Substance ID)

C88X29Y479

LYCOPODIUM CLAVATUM SPORE

RxCUI 283577

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "C88X29Y479",
    "rxcui": "283577",
    "inchikey": null,
    "display_name": "LYCOPODIUM CLAVATUM SPORE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "0403922e-dce1-4925-8877-d6b765f7fc18": {
      "match": "brand_token",
      "title": "LYCOPODIUM COMBINATION 9231 (LYCOPODIUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-1783_ec0c31ec-1971-7332-e053-2a95a90abc0a",
  "productndc": "37662-1783",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LYCOPODIUM CLAVATUM SPORE",
  "proprietary_name": "Lycopodium Clavatum",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Lycopodium Clavatum",
  "start_marketing_date": "20221027",
  "active_numerator_strength": "10"
}

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