Magnesia Nitrica

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
3766232001
200 PELLET in 1 VIAL, GLASS (37662-3200-1)
ndc11
3766232002
500 PELLET in 1 VIAL, GLASS (37662-3200-2)
ndc11
3766232003
3000 PELLET in 1 BOTTLE, GLASS (37662-3200-3)
ndc11
3766232004
10000 PELLET in 1 BOTTLE, GLASS (37662-3200-4)

Annotations

UNII (FDA Substance ID)

05MVC8T5JN

MAGNESIUM NITRITE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "05MVC8T5JN",
    "rxcui": null,
    "inchikey": "AAJBNRZDTJPMTJ-UHFFFAOYSA-L",
    "display_name": "MAGNESIUM NITRITE",
    "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": "37662-3200_fbed7a68-25a8-c411-e053-6394a90acee7",
  "productndc": "37662-3200",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MAGNESIUM NITRITE",
  "proprietary_name": "Magnesia Nitrica",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Magnesia Nitrica",
  "start_marketing_date": "20230517",
  "active_numerator_strength": "100"
}

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