Coccus Cacti

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
3766204911
80 PELLET in 1 VIAL, GLASS (37662-0491-1)
ndc11
3766204912
200 PELLET in 1 VIAL, GLASS (37662-0491-2)
ndc11
3766204913
1200 PELLET in 1 BOTTLE, GLASS (37662-0491-3)
ndc11
3766204914
4000 PELLET in 1 BOTTLE, GLASS (37662-0491-4)

Annotations

UNII (FDA Substance ID)

LZB7TFX1LT

PROTORTONIA CACTI

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "LZB7TFX1LT",
    "rxcui": null,
    "inchikey": null,
    "display_name": "PROTORTONIA CACTI",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "853c7464-f6cf-2bba-e053-2991aa0a7030": {
      "match": "brand_token",
      "title": "COCCUS CACTI (PROTORTONIA CACTI\t) PELLET [BOIRON]",
      "spl_version": "2",
      "published_date": "2023-11-10"
    }
  },
  "productid": "37662-0491_e12191cb-db2b-2f9d-e053-2a95a90a7110",
  "productndc": "37662-0491",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PROTORTONIA CACTI",
  "proprietary_name": "Coccus Cacti",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Coccus Cacti",
  "start_marketing_date": "20220610",
  "active_numerator_strength": "30"
}

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