Magnesia Bromata

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
3766226711
80 PELLET in 1 VIAL, GLASS (37662-2671-1)
ndc11
3766226712
200 PELLET in 1 VIAL, GLASS (37662-2671-2)
ndc11
3766226713
1200 PELLET in 1 BOTTLE, GLASS (37662-2671-3)
ndc11
3766226714
4000 PELLET in 1 BOTTLE, GLASS (37662-2671-4)

Annotations

UNII (FDA Substance ID)

370X21564P

MAGNESIUM BROMATE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "370X21564P",
    "rxcui": null,
    "inchikey": "RNUHOKZSYYKPPI-UHFFFAOYSA-L",
    "display_name": "MAGNESIUM BROMATE",
    "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": "37662-2671_f44ed0ee-1e6c-2add-e053-2a95a90a1665",
  "productndc": "37662-2671",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MAGNESIUM BROMATE",
  "proprietary_name": "Magnesia Bromata",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Magnesia Bromata",
  "start_marketing_date": "20230209",
  "active_numerator_strength": "30"
}

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