Rhus Glabra

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 · 3

ndc11
3766213721
200 PELLET in 1 VIAL, GLASS (37662-1372-1)
ndc11
3766213722
1200 PELLET in 1 BOTTLE, GLASS (37662-1372-2)
ndc11
3766213723
4000 PELLET in 1 BOTTLE, GLASS (37662-1372-3)

Annotations

UNII (FDA Substance ID)

RHH784E0K6

RHUS GLABRA TOP

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "RHH784E0K6",
    "rxcui": null,
    "inchikey": null,
    "display_name": "RHUS GLABRA TOP",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "a176c241-fc2d-4fea-82d9-81183971b4cf": {
      "match": "brand_token",
      "title": "RHUS ACONITUM LIQUID [URIEL PHARMACY INC.]",
      "spl_version": "5",
      "published_date": "2026-03-02"
    }
  },
  "productid": "37662-1372_e68d0227-13a9-c6be-e053-2a95a90aacbd",
  "productndc": "37662-1372",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "RHUS GLABRA TOP",
  "proprietary_name": "Rhus Glabra",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Rhus Glabra",
  "start_marketing_date": "20220818",
  "active_numerator_strength": "6"
}

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