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United States · US · US:0220-0774_09ba5762-6b48-3a9b-e063-6394a90a53e9

Baptisia tinctoria

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBoiron
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0220077441
    9 [hp_C] in 1 TUBE (0220-0774-41)

Annotations

UNII (FDA Substance ID)
5EF0HWI5WU
BAPTISIA TINCTORIA ROOT
RxCUI 1309779
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "5EF0HWI5WU",
    "rxcui": "1309779",
    "inchikey": null,
    "display_name": "BAPTISIA TINCTORIA ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "dead18ed-a4ba-8129-e053-2a95a90a3f2e": {
      "match": "brand_token",
      "title": "BAPTISIA TINCTORIA KIT REFILL (BAPTISIA TINCTORIA ROOT) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]",
      "spl_version": "4",
      "published_date": "2025-01-30"
    }
  },
  "productid": "0220-0774_09ba5762-6b48-3a9b-e063-6394a90a53e9",
  "productndc": "0220-0774",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BAPTISIA TINCTORIA ROOT",
  "proprietary_name": "Baptisia tinctoria",
  "active_ingred_unit": "[hp_C]/9[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "BAPTISIA TINCTORIA ROOT",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "9"
}

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