Thuja occidentalis

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerNewton Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5571490141
28 g in 1 BOTTLE, GLASS (55714-9014-1)

Annotations

UNII (FDA Substance ID)

1NT28V9397

THUJA OCCIDENTALIS LEAFY TWIG

RxCUI 1309754

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "1NT28V9397",
    "rxcui": "1309754",
    "inchikey": null,
    "display_name": "THUJA OCCIDENTALIS LEAFY TWIG",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "11364528-399d-4f64-a682-ec8f503af0aa": {
      "match": "brand_token",
      "title": "THUJA OCCIDENTALIS 7140 (THUJA OCCIDENTALIS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "55714-9014_2dd2175c-db42-4df9-e063-6394a90a5e84",
  "productndc": "55714-9014",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "THUJA OCCIDENTALIS LEAFY TWIG",
  "proprietary_name": "Thuja occidentalis",
  "active_ingred_unit": "[hp_C]/g",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Thuja occidentalis",
  "start_marketing_date": "20200101",
  "active_numerator_strength": "30"
}

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