Baptisia Tinctoria Kit Refill

UNIISPL

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

Identification

ManufacturerWashington Homeopathic Products

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7191976501
350 PELLET in 1 VIAL, GLASS (71919-765-01)

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": "71919-765_2cc7eaaf-e2c6-f06a-e063-6394a90a1961",
  "productndc": "71919-765",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BAPTISIA TINCTORIA ROOT",
  "proprietary_name": "Baptisia Tinctoria Kit Refill",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "BAPTISIA TINCTORIA ROOT",
  "start_marketing_date": "20220510",
  "active_numerator_strength": "200"
}

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