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 · 4

ndc11
6354535601
200 PELLET in 1 VIAL, GLASS (63545-356-01)
ndc11
6354535602
500 PELLET in 1 VIAL, GLASS (63545-356-02)
ndc11
6354535603
3000 PELLET in 1 BOTTLE, GLASS (63545-356-03)
ndc11
6354535604
10000 PELLET in 1 BOTTLE, GLASS (63545-356-04)

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": "63545-356_c562c423-70e5-0953-e053-2a95a90a6681",
  "productndc": "63545-356",
  "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": "200"
}

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