Quercus Rubra Glandium

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
3766233011
200 PELLET in 1 VIAL, GLASS (37662-3301-1)
ndc11
3766233012
500 PELLET in 1 VIAL, GLASS (37662-3301-2)
ndc11
3766233013
3000 PELLET in 1 BOTTLE, GLASS (37662-3301-3)
ndc11
3766233014
10000 PELLET in 1 BOTTLE, GLASS (37662-3301-4)

Annotations

UNII (FDA Substance ID)

UQ0Z34X16U

QUERCUS RUBRA WHOLE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "UQ0Z34X16U",
    "rxcui": null,
    "inchikey": null,
    "display_name": "QUERCUS RUBRA WHOLE",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "44fe7178-e641-04ce-e063-6394a90a614e": {
      "match": "brand_token",
      "title": "QUERCUS RADIX-CINIS 9X LIQUID [TRUE BOTANICA, LLC]",
      "spl_version": "1",
      "published_date": "2025-12-09"
    }
  },
  "productid": "37662-3301_fd2ecde0-2970-060f-e053-6294a90afd98",
  "productndc": "37662-3301",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "QUERCUS RUBRA WHOLE",
  "proprietary_name": "Quercus Rubra Glandium",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Quercus Rubra Glandium",
  "start_marketing_date": "20230602",
  "active_numerator_strength": "1"
}

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