Baptisia Tinctoria

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
6354535201
200 PELLET in 1 VIAL, GLASS (63545-352-01)
ndc11
6354535202
1200 PELLET in 1 BOTTLE, GLASS (63545-352-02)
ndc11
6354535203
4000 PELLET in 1 BOTTLE, GLASS (63545-352-03)

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": "63545-352_c562c423-70e5-0953-e053-2a95a90a6681",
  "productndc": "63545-352",
  "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]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Baptisia Tinctoria",
  "start_marketing_date": "20210622",
  "active_numerator_strength": "6"
}

Access this data programmatically

Query Baptisia Tinctoria and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.

Get a free API key Read the API docs