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United States · US · US:37662-2649_f425d971-94c6-57c8-e053-2995a90aa8cd
Magnesia Arsenata
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHahnemann Laboratories, INC.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc113766226491200 PELLET in 1 VIAL, GLASS (37662-2649-1)
- ndc113766226492500 PELLET in 1 VIAL, GLASS (37662-2649-2)
- ndc1137662264933000 PELLET in 1 BOTTLE, GLASS (37662-2649-3)
- ndc11376622649410000 PELLET in 1 BOTTLE, GLASS (37662-2649-4)
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": "37662-2649_f425d971-94c6-57c8-e053-2995a90aa8cd",
"productndc": "37662-2649",
"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": "200"
}Access this data programmatically
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