Collinsonia Canadensis

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 · 3

ndc11
3766204811
200 PELLET in 1 VIAL, GLASS (37662-0481-1)
ndc11
3766204812
1200 PELLET in 1 BOTTLE, GLASS (37662-0481-2)
ndc11
3766204813
4000 PELLET in 1 BOTTLE, GLASS (37662-0481-3)

Annotations

UNII (FDA Substance ID)

O2630F3XDR

COLLINSONIA CANADENSIS ROOT

RxCUI 1309782

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "O2630F3XDR",
    "rxcui": "1309782",
    "inchikey": null,
    "display_name": "COLLINSONIA CANADENSIS ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "6854bbd6-67e6-12c5-e053-2991aa0a1f7c": {
      "match": "brand_token",
      "title": "COLLINSONIA CANADENSIS (COLLINSONIA CANADENSIS ROOT) PELLET [BOIRON]",
      "spl_version": "4",
      "published_date": "2026-02-12"
    }
  },
  "productid": "37662-0481_e120ae15-273e-f3cd-e053-2a95a90a9d0e",
  "productndc": "37662-0481",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "COLLINSONIA CANADENSIS ROOT",
  "proprietary_name": "Collinsonia Canadensis",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Collinsonia Canadensis",
  "start_marketing_date": "20220610",
  "active_numerator_strength": "6"
}

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