Strontium Sulphuricum

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
3766240601
200 PELLET in 1 VIAL, GLASS (37662-4060-1)
ndc11
3766240602
500 PELLET in 1 VIAL, GLASS (37662-4060-2)
ndc11
3766240603
3000 PELLET in 1 BOTTLE, GLASS (37662-4060-3)
ndc11
3766240604
10000 PELLET in 1 BOTTLE, GLASS (37662-4060-4)

Annotations

UNII (FDA Substance ID)

7Q3KX2L47F

STRONTIUM SULFATE

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "7Q3KX2L47F",
    "rxcui": null,
    "inchikey": "UBXAKNTVXQMEAG-UHFFFAOYSA-L",
    "display_name": "STRONTIUM SULFATE",
    "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": "37662-4060_0675be77-6cc0-5126-e063-6394a90ad6ed",
  "productndc": "37662-4060",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "STRONTIUM SULFATE",
  "proprietary_name": "Strontium Sulphuricum",
  "active_ingred_unit": "[hp_C]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Strontium Sulphuricum",
  "start_marketing_date": "20230928",
  "active_numerator_strength": "500"
}

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