Rumex Crispus

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
3766220041
200 PELLET in 1 VIAL, GLASS (37662-2004-1)
ndc11
3766220042
500 PELLET in 1 VIAL, GLASS (37662-2004-2)
ndc11
3766220043
3000 PELLET in 1 BOTTLE, GLASS (37662-2004-3)
ndc11
3766220044
10000 PELLET in 1 BOTTLE, GLASS (37662-2004-4)

Annotations

UNII (FDA Substance ID)

9N1RM2S62C

RUMEX CRISPUS ROOT

RxCUI 1345677

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "9N1RM2S62C",
    "rxcui": "1345677",
    "inchikey": null,
    "display_name": "RUMEX CRISPUS ROOT",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "86bb315a-990c-b13d-e053-2991aa0a1eb2": {
      "match": "brand_token",
      "title": "RUMEX CRISPUS (RUMEX CRISPUS ROOT\t) PELLET [BOIRON]",
      "spl_version": "2",
      "published_date": "2023-11-15"
    }
  },
  "productid": "37662-2004_ee1ad771-9548-4272-e053-2a95a90aacc4",
  "productndc": "37662-2004",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "RUMEX CRISPUS ROOT",
  "proprietary_name": "Rumex Crispus",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Rumex Crispus",
  "start_marketing_date": "20221122",
  "active_numerator_strength": "100"
}

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