Celestite 6X

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerTrue Botanica, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5364519016
30 mL in 1 BOTTLE (53645-1901-6)

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": {
    "1a50b46b-834b-bd18-e063-6394a90a58e5": {
      "match": "brand_token",
      "title": "CELESTITE 6X LIQUID [TRUE BOTANICA, LLC]",
      "spl_version": "1",
      "published_date": "2024-07-03"
    }
  },
  "productid": "53645-1901_1a50af81-4251-aa0d-e063-6394a90a5187",
  "productndc": "53645-1901",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "STRONTIUM SULFATE",
  "proprietary_name": "Celestite 6X",
  "active_ingred_unit": "[hp_X]/30mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Celestite 6X",
  "start_marketing_date": "20240624",
  "active_numerator_strength": "6"
}

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