Aluminium Carbonicum

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
3766235111
200 PELLET in 1 VIAL, GLASS (37662-3511-1)
ndc11
3766235112
500 PELLET in 1 VIAL, GLASS (37662-3511-2)
ndc11
3766235113
3000 PELLET in 1 BOTTLE, GLASS (37662-3511-3)
ndc11
3766235114
10000 PELLET in 1 BOTTLE, GLASS (37662-3511-4)

Annotations

UNII (FDA Substance ID)

1GA689N629

ALUMINUM CARBONATE

RxCUI 89858

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "1GA689N629",
    "rxcui": "89858",
    "inchikey": "PPQREHKVAOVYBT-UHFFFAOYSA-H",
    "display_name": "ALUMINUM CARBONATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "a474ba15-34a5-f07e-e053-2995a90a61ca": {
      "match": "brand_token",
      "title": "ALUMINIUM SULPHURICUM PELLET [HAHNEMANN LABORATORIES, INC.]",
      "spl_version": "3",
      "published_date": "2025-01-13"
    }
  },
  "productid": "37662-3511_ffc56a39-0f70-2879-e053-6394a90a3a4a",
  "productndc": "37662-3511",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALUMINUM CARBONATE",
  "proprietary_name": "Aluminium Carbonicum",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Aluminium Carbonicum",
  "start_marketing_date": "20230630",
  "active_numerator_strength": "10"
}

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