Kalmia Latifolia

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
3766209001
80 PELLET in 1 VIAL, GLASS (37662-0900-1)
ndc11
3766209002
200 PELLET in 1 VIAL, GLASS (37662-0900-2)
ndc11
3766209003
1200 PELLET in 1 BOTTLE, GLASS (37662-0900-3)
ndc11
3766209004
4000 PELLET in 1 BOTTLE, GLASS (37662-0900-4)

Annotations

UNII (FDA Substance ID)

79N6542N18

KALMIA LATIFOLIA LEAF

RxCUI 1307972

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "79N6542N18",
    "rxcui": "1307972",
    "inchikey": null,
    "display_name": "KALMIA LATIFOLIA LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3b3c955d-453e-28e2-e063-6394a90a6bf9": {
      "match": "brand_token",
      "title": "KALMIA (ARNICA MONTANA, CHELIDONIUM, COLCHICUM, KALMIA, RANUNCULUS BULB, SANGUINARIA NIT, SUMBUL) LIQUID [BM PRIVATE LIMITED]",
      "spl_version": "2",
      "published_date": "2026-02-17"
    }
  },
  "productid": "37662-0900_e3cbb973-4e7a-ce48-e053-2995a90abe02",
  "productndc": "37662-0900",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "KALMIA LATIFOLIA LEAF",
  "proprietary_name": "Kalmia Latifolia",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Kalmia Latifolia",
  "start_marketing_date": "20220714",
  "active_numerator_strength": "30"
}

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