AMMON CARBON

UNIISPL

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

Identification

ManufacturerRxhomeo Private Limited d.b.a. Rxhomeo, Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
1563125780
10 mL in 1 BOTTLE (15631-2578-0)
ndc11
1563125781
30 mL in 1 BOTTLE (15631-2578-1)

Annotations

UNII (FDA Substance ID)

NJ5VT0FKLJ

AMMONIUM CARBONATE

RxCUI 1310190

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "NJ5VT0FKLJ",
    "rxcui": "1310190",
    "inchikey": null,
    "display_name": "AMMONIUM CARBONATE",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "1996c0e8-131e-cdef-e063-6394a90a9df8": {
      "match": "brand_token",
      "title": "AMMON CARBON LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]",
      "spl_version": "1",
      "published_date": "2024-06-12"
    }
  },
  "productid": "15631-2578_1996c8ac-4bc8-1e1e-e063-6394a90a3ac3",
  "productndc": "15631-2578",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AMMONIUM CARBONATE",
  "proprietary_name": "AMMON CARBON",
  "active_ingred_unit": "[hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "AMMON CARBON",
  "start_marketing_date": "20240523",
  "active_numerator_strength": "3"
}

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