Acidum Oxalicum

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
3766225201
200 PELLET in 1 VIAL, GLASS (37662-2520-1)
ndc11
3766225202
500 PELLET in 1 VIAL, GLASS (37662-2520-2)
ndc11
3766225203
3000 PELLET in 1 BOTTLE, GLASS (37662-2520-3)
ndc11
3766225204
10000 PELLET in 1 BOTTLE, GLASS (37662-2520-4)

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": {
    "9a6711a9-e0a4-9083-e053-2a95a90ad4a4": {
      "match": "brand_token",
      "title": "ACIDUM ACETICUM PELLET [HAHNEMANN LABORATORIES, INC.]",
      "spl_version": "25",
      "published_date": "2025-01-13"
    }
  },
  "productid": "37662-2520_f323df0f-a3ff-6230-e053-2995a90a6252",
  "productndc": "37662-2520",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OXALIC ACID DIHYDRATE",
  "proprietary_name": "Acidum Oxalicum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Acidum Oxalicum",
  "start_marketing_date": "20230125",
  "active_numerator_strength": "500"
}

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