Strontium 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
3766230581
200 PELLET in 1 VIAL, GLASS (37662-3058-1)
ndc11
3766230582
500 PELLET in 1 VIAL, GLASS (37662-3058-2)
ndc11
3766230583
3000 PELLET in 1 BOTTLE, GLASS (37662-3058-3)
ndc11
3766230584
10000 PELLET in 1 BOTTLE, GLASS (37662-3058-4)

Annotations

UNII (FDA Substance ID)

EFY8GJS81Z

STRONTIUM FLUORIDE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "EFY8GJS81Z",
    "rxcui": null,
    "inchikey": "FVRNDBHWWSPNOM-UHFFFAOYSA-L",
    "display_name": "STRONTIUM FLUORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "86a59e96-d358-3644-e053-2a91aa0a186a": {
      "match": "brand_token",
      "title": "STRONTIUM CARBONICUM (STRONTIUM CARBONATE) PELLET [BOIRON]",
      "spl_version": "2",
      "published_date": "2023-11-16"
    }
  },
  "productid": "37662-3058_fa5b126b-5bc7-a682-e053-6294a90adb7f",
  "productndc": "37662-3058",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "STRONTIUM FLUORIDE",
  "proprietary_name": "Strontium Fluoratum",
  "active_ingred_unit": "[hp_M]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Strontium Fluoratum",
  "start_marketing_date": "20230427",
  "active_numerator_strength": "1"
}

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