Oxalicum acidum

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBoiron

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0220384241
30 [hp_C] in 1 TUBE (0220-3842-41)

Annotations

UNII (FDA Substance ID)

0K2L2IJ59O

OXALIC ACID DIHYDRATE

RxCUI 1427057

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "0K2L2IJ59O",
    "rxcui": "1427057",
    "inchikey": "GEVPUGOOGXGPIO-UHFFFAOYSA-N",
    "display_name": "OXALIC ACID DIHYDRATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3a9d4e84-118e-0eca-e063-6294a90a73cc": {
      "match": "brand_token",
      "title": "OXALICUM ACIDUM (OXALIC ACID DIHYDRATE) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2025-08-20"
    }
  },
  "productid": "0220-3842_0a211521-c517-7c84-e063-6294a90a0a8a",
  "productndc": "0220-3842",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OXALIC ACID DIHYDRATE",
  "proprietary_name": "Oxalicum acidum",
  "active_ingred_unit": "[hp_C]/30[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "OXALIC ACID DIHYDRATE",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "30"
}

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