Plumeria Rubra

UNII

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
3766233471
200 PELLET in 1 VIAL, GLASS (37662-3347-1)
ndc11
3766233472
500 PELLET in 1 VIAL, GLASS (37662-3347-2)
ndc11
3766233473
3000 PELLET in 1 BOTTLE, GLASS (37662-3347-3)
ndc11
3766233474
10000 PELLET in 1 BOTTLE, GLASS (37662-3347-4)

Annotations

UNII (FDA Substance ID)

31FL06Y50D

PLUMERIA RUBRA WHOLE

Raw payload (JSON)

{
  "unii": {
    "unii": "31FL06Y50D",
    "rxcui": null,
    "inchikey": null,
    "display_name": "PLUMERIA RUBRA WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "productid": "37662-3347_fe101e58-b959-14ec-e053-6294a90a6118",
  "productndc": "37662-3347",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "PLUMERIA RUBRA WHOLE",
  "proprietary_name": "Plumeria Rubra",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Plumeria Rubra",
  "start_marketing_date": "20230613",
  "active_numerator_strength": "200"
}

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