Magnesia Arsenata

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
3766226471
80 PELLET in 1 VIAL, GLASS (37662-2647-1)
ndc11
3766226472
200 PELLET in 1 VIAL, GLASS (37662-2647-2)
ndc11
3766226473
1200 PELLET in 1 BOTTLE, GLASS (37662-2647-3)
ndc11
3766226474
4000 PELLET in 1 BOTTLE, GLASS (37662-2647-4)

Annotations

UNII (FDA Substance ID)

I15RML7CUZ

MAGNESIUM ARSENATE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "I15RML7CUZ",
    "rxcui": null,
    "inchikey": "WFJMDQBZLSODEP-UHFFFAOYSA-H",
    "display_name": "MAGNESIUM ARSENATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "de5e63c1-d70e-496d-bfe2-629642a3ebd0": {
      "match": "brand_token",
      "title": "MAGNESIA PHOSPHORICA 8008 (MAGNESIA PHOSPHORICA) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
      "spl_version": "2",
      "published_date": "2026-01-12"
    }
  },
  "productid": "37662-2647_f425d971-94c6-57c8-e053-2995a90aa8cd",
  "productndc": "37662-2647",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MAGNESIUM ARSENATE",
  "proprietary_name": "Magnesia Arsenata",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Magnesia Arsenata",
  "start_marketing_date": "20230207",
  "active_numerator_strength": "30"
}

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