Gelsemium Sempervirens

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
3766209231
80 PELLET in 1 VIAL, GLASS (37662-0923-1)
ndc11
3766209232
200 PELLET in 1 VIAL, GLASS (37662-0923-2)
ndc11
3766209233
1200 PELLET in 1 BOTTLE, GLASS (37662-0923-3)
ndc11
3766209234
4000 PELLET in 1 BOTTLE, GLASS (37662-0923-4)

Annotations

UNII (FDA Substance ID)

639KR60Q1Q

GELSEMIUM SEMPERVIRENS ROOT

RxCUI 1309695

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "639KR60Q1Q",
    "rxcui": "1309695",
    "inchikey": null,
    "display_name": "GELSEMIUM SEMPERVIRENS ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "9790600a-929b-48ce-af11-4b7157c2d31a": {
      "match": "brand_token",
      "title": "GELSEMIUM COMBINATION 9223 (GELSEMIUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-0923_e3dc20b9-1e39-47df-e053-2995a90abc04",
  "productndc": "37662-0923",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "GELSEMIUM SEMPERVIRENS ROOT",
  "proprietary_name": "Gelsemium Sempervirens",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Gelsemium Sempervirens",
  "start_marketing_date": "20220715",
  "active_numerator_strength": "30"
}

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