Rhododendron Chrysanthum

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
3766240061
200 PELLET in 1 VIAL, GLASS (37662-4006-1)
ndc11
3766240062
500 PELLET in 1 VIAL, GLASS (37662-4006-2)
ndc11
3766240063
3000 PELLET in 1 BOTTLE, GLASS (37662-4006-3)
ndc11
3766240064
10000 PELLET in 1 BOTTLE, GLASS (37662-4006-4)

Annotations

UNII (FDA Substance ID)

IV92NQJ73U

RHODODENDRON AUREUM LEAF

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "IV92NQJ73U",
    "rxcui": null,
    "inchikey": null,
    "display_name": "RHODODENDRON AUREUM LEAF",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "9a3d93c9-261d-4711-ad75-8e4c1f87c936": {
      "match": "brand_token",
      "title": "RHODODENDRON COMBINATION 9241 (RHODODENDRON COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-4006_05fc5431-1b3d-a47a-e063-6394a90a8baf",
  "productndc": "37662-4006",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "RHODODENDRON AUREUM LEAF",
  "proprietary_name": "Rhododendron Chrysanthum",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Rhododendron Chrysanthum",
  "start_marketing_date": "20230922",
  "active_numerator_strength": "10"
}

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