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United States· US:87674-100_558261cb-4904-6f03-e063-6394a90a58e1

The Cell Salt Co. Daily Blend 12 in 1

A medicinal product containing ferrosoferric phosphate; sodium sulfate; calcium sulfate anhydrous; calcium fluoride; silicon dioxide; potassium chloride; sodium chloride; magnesium phosphate, dibasic trihydrate; sodium phosphate, dibasic, heptahydrate; potassium phosphate; potassium sulfate; tribasic calcium phosphate, registered in United States by The Cell Salt Company LLC.

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedThe Cell Salt Co. Daily Blend 12 in 1ATC—REGISTER NO.US:87674-100_558261cb…PACKS LISTED1CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
FERROSOFERRIC PHOSPHATE; SODIUM SULFATE; CALCIUM SULFATE ANHYDROUS; CALCIUM FLUORIDE; SILICON DIOXIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; POTASSIUM PHOSPHATE; POTASSIUM SULFATE; TRIBASIC CALCIUM PHOSPHATE
Manufacturer
The Cell Salt Company LLC
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 1

  • ndc11
    87674-100-10

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/4d76e2e0-da89-481d-b966-1dada271d02d
GET /v1/drugs/4d76e2e0-da89-481d-b966-1dada271d02d?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "ORAL",
  "source": "ndc",
  "strength": "12; 6; 6; 12; 12; 6; 6; 6; 6; 6; 6; 6",
  "substance": "FERROSOFERRIC PHOSPHATE; SODIUM SULFATE; CALCIUM SULFATE ANHYDROUS; CALCIUM FLUORIDE; SILICON DIOXIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; POTASSIUM PHOSPHATE; POTASSIUM SULFATE; TRIBASIC CALCIUM PHOSPHATE",
  "productndc": "87674-100",
  "dosage_form": "TABLET, SOLUBLE",
  "dea_schedule": null,
  "strength_unit": "[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC"
}

See everything about ferrosoferric phosphate; sodium sulfate; calcium sulfate anhydrous; calcium fluoride; silicon dioxide; potassium chloride; sodium chloride; magnesium phosphate, dibasic trihydrate; sodium phosphate, dibasic, heptahydrate; potassium phosphate; potassium sulfate; tribasic calcium phosphate.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.