Echinacea Angustifolia

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
3766206651
200 PELLET in 1 VIAL, GLASS (37662-0665-1)
ndc11
3766206652
1200 PELLET in 1 BOTTLE, GLASS (37662-0665-2)
ndc11
3766206653
4000 PELLET in 1 BOTTLE, GLASS (37662-0665-3)

Annotations

UNII (FDA Substance ID)

VB06AV5US8

ECHINACEA ANGUSTIFOLIA WHOLE

RxCUI 236121

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "VB06AV5US8",
    "rxcui": "236121",
    "inchikey": null,
    "display_name": "ECHINACEA ANGUSTIFOLIA WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "7efadb70-99e4-428b-a8ef-a2797327c6fa": {
      "match": "brand_token",
      "title": "ECHINACEA (ECHINACEA ANGUSTIFOLIA, HAMAMMELIS VIRGINIANA, CALCAREA PHOSPHORICA, HYDRASTIS CANADANESIS, SENEGA OFFICINALIS, SILICEA, CONIUM, AURUM MURIATICUM NATRONATUM, CALCAREA CARBONICA, FUCUS VESICULOSUS, LACHESIS MUTUS) TABLET, ORALLY DISINTEGRATING [MARCO PHARMA INTERNATIONAL LLC.]",
      "spl_version": "7",
      "published_date": "2026-01-14"
    }
  },
  "productid": "37662-0665_e1fa828f-be29-0fa0-e053-2a95a90a2f91",
  "productndc": "37662-0665",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ECHINACEA ANGUSTIFOLIA WHOLE",
  "proprietary_name": "Echinacea Angustifolia",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Echinacea Angustifolia",
  "start_marketing_date": "20220621",
  "active_numerator_strength": "6"
}

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