Magnesia Fluorata

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
3766226641
200 PELLET in 1 VIAL, GLASS (37662-2664-1)
ndc11
3766226642
500 PELLET in 1 VIAL, GLASS (37662-2664-2)
ndc11
3766226643
3000 PELLET in 1 BOTTLE, GLASS (37662-2664-3)
ndc11
3766226644
10000 PELLET in 1 BOTTLE, GLASS (37662-2664-4)

Annotations

UNII (FDA Substance ID)

5N014C7IWU

MAGNESIUM FLUORIDE

RxCUI 1435860

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "5N014C7IWU",
    "rxcui": "1435860",
    "inchikey": "ORUIBWPALBXDOA-UHFFFAOYSA-L",
    "display_name": "MAGNESIUM FLUORIDE",
    "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": "37662-2664_f44b5405-566f-6a32-e053-2995a90aa387",
  "productndc": "37662-2664",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MAGNESIUM FLUORIDE",
  "proprietary_name": "Magnesia Fluorata",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Magnesia Fluorata",
  "start_marketing_date": "20230209",
  "active_numerator_strength": "100"
}

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