United States· US:48433-230_3d1d89c5-85de-4aa8-9145-5ec6a25983ce
Strong Iodine Solution
A medicinal product containing iodine; potassium iodide, registered in United States by Safecor Health, LLC.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- IODINE; POTASSIUM IODIDE
- Manufacturer
- Safecor Health, 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 · 2
- ndc11484332301514 mL in 1 BOTTLE (48433-230-15)
- ndc1148433-230-15
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Iodine; potassium iodide in 4 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomIodine 1% aqueous topical solutionSpecial Order
- IrelandIodine Liniment Strong, Cutaneous Solution Iodine 10% w/v Potassium Iodide 6% w/vOvelle Limited
- CanadaSTRONGER IODINE TCTDOMINION VETERINARY LABORATORIES LTD.
- PolandSolutio Iodi Cum Glycerini Coel (płyn lugola)Wytwórnia Euceryny Laboratorium Farmaceutyczne COEL S.J. E.Z.M. Konstanty
Authorised across Europe · EMA
The same active substance is authorised in 4 EEA countries. Names it is sold under:
- United Kingdom (Northern Ireland) · Alcoholic Iodine, Aqueous Iodine Thornton & Ross
- Ireland · Iodine Liniment Strong, Iodine Tincture (Alcoholic Iodine Solution Bp)
- Italy · Iodio Almus, Iodio Marco Viti
- Malta · Iodine Laboratorio Chimico Farmaceutico A.Sella
Source: European Medicines Agency, Article 57 product data.
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/713c2017-8bf9-4269-9cac-1d5977c1e310 GET /v1/drugs/713c2017-8bf9-4269-9cac-1d5977c1e310?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": "700; 1400",
"substance": "IODINE; POTASSIUM IODIDE",
"productndc": "48433-230",
"dosage_form": "SOLUTION/ DROPS",
"dea_schedule": null,
"strength_unit": "mg/mL; mg/mL",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER"
}See everything about iodine; potassium iodide.
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.