United States· US:0436-0669_4b0adcc9-ddf5-aeb4-e063-6294a90aafab
Di-Dak-Sol
A sodium hypochlorite product containing sodium hypochlorite, registered in United States by Century Pharmaceuticals, Inc.. The same ATC class is registered in 4 of our 19 countries.
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
Where it is registered
Sodium hypochlorite is registered in 4 of 19 countries.
Countries holding a registration under ATC D08AX07 (sodium hypochlorite), each read from that country’s own register.
- This record: United States, from FDA National Drug Code directory (United States)
- 2 of them publish a price we can compare per daily dose
Sodium hypochlorite · ATC D08AX07
4 / 19 countries
- Germany
- Switzerlandprice
- United Kingdom
- United Statesprice
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- SODIUM HYPOCHLORITE
- Manufacturer
- Century Pharmaceuticals, Inc.
- Country
- United States (US)
- ATC code
- D08AX07
- ATC class
- Sodium hypochlorite
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- September 27, 2026
Packs & prices · 2
- ndc110436066916473 mL in 1 BOTTLE (0436-0669-16)
- ndc110436-0669-16
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sodium hypochlorite in 6 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- CanadaADVANCE 12AADVANCE CHEMICALS LTD.
- United KingdomMilton No.2 sterilising fluidCeuta Healthcare Ltd
- Japan次亜塩素酸ナトリウムヤクハン製薬
- GermanyHistolithLege Artis Pharma Gmbh + Co. Kg
- FranceAMUKINE 0,06 %, solution pour application cutanéeGIFRER BARBEZAT
- BelgiumDakin Cooper 0.5 g/100 mlVemedia Manufacturing
Authorised across Europe · EMA
The same active substance is authorised in 2 EEA countries. Names it is sold under:
- Germany · Histolith, Hypochlorit Speiko
- Italy · Amukine Med
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/da154124-6184-4231-8f95-5195fdceae17 GET /v1/drugs/da154124-6184-4231-8f95-5195fdceae17?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": "TOPICAL",
"source": "ndc",
"strength": ".125",
"substance": "SODIUM HYPOCHLORITE",
"productndc": "0436-0669",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"strength_unit": "mg/mL",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER"
}See everything about sodium hypochlorite.
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.