Manganum Fluoratum

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
3766228501
200 PELLET in 1 VIAL, GLASS (37662-2850-1)
ndc11
3766228502
500 PELLET in 1 VIAL, GLASS (37662-2850-2)
ndc11
3766228503
3000 PELLET in 1 BOTTLE, GLASS (37662-2850-3)
ndc11
3766228504
10000 PELLET in 1 BOTTLE, GLASS (37662-2850-4)

Annotations

UNII (FDA Substance ID)

1XRA8Q11QP

MANGANESE DIFLUORIDE

RxCUI 1921126

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "1XRA8Q11QP",
    "rxcui": "1921126",
    "inchikey": "CTNMMTCXUUFYAP-UHFFFAOYSA-L",
    "display_name": "MANGANESE DIFLUORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3aae2fe5-08a7-1b9f-e063-6394a90aff69": {
      "match": "brand_token",
      "title": "MANGANUM METALLICUM (MANGANESE) PELLET [BOIRON]",
      "spl_version": "1",
      "published_date": "2025-07-28"
    }
  },
  "productid": "37662-2850_f788fe1a-9b19-9f67-e053-6294a90ae563",
  "productndc": "37662-2850",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "MANGANESE DIFLUORIDE",
  "proprietary_name": "Manganum Fluoratum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Manganum Fluoratum",
  "start_marketing_date": "20230327",
  "active_numerator_strength": "200"
}

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