United States· US:68062-2219_48dfd908-1e99-cc98-e063-6294a90ac9bc

VitaVie

A medicinal product containing benzalkonium chloride, registered in United States by Spa De Soleil.

US label

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

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedVitaVieATC—REGISTER NO.US:68062-2219_48dfd90…PACKS LISTED4CHECKEDAugust 23, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
BENZALKONIUM CHLORIDE
Manufacturer
Spa De Soleil
Country
United States (US)
ATC code
—
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
August 23, 2026

Packs & prices · 4

  • ndc11
    68062-2219-1
  • ndc11
    68062-2219-2
  • ndc11
    6806222191
    240 mL in 1 BOTTLE, PUMP (68062-2219-1)
  • ndc11
    6806222192
    1893 mL in 1 BOTTLE, PUMP (68062-2219-2)

Regulatory notes

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

Same medicine, other countries

Benzalkonium chloride in 6 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All benzalkonium chloride products

Authorised across Europe · EMA

The same active substance is authorised in 15 EEA countries. Names it is sold under:

  • Belgium · Cedium, Cedium Benzalkonium
  • Bulgaria · Фарматекс
  • Czechia · Dettol, Septolete D
  • Spain · Ginejuvent
  • France · Humex Fournier
  • United Kingdom (Northern Ireland) · Dermax, Dettol Med
  • Greece · Dettox Wound
  • Italy · Benalcon, Citrosil
  • Luxembourg · Cedium, Cedium Benzalkonium
  • Netherlands · Dettol Med
  • Poland · Septolete, Septolete D
  • Portugal · Detolpro
  • Romania · Contracept-M
  • Slovenia · Septolete D Z Okusom Mentola, Septolete Z Okusom Mentola
  • Slovakia · Dettol

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/ea8a5ce3-dccb-49c7-9560-fc4dbb07b99a
GET /v1/drugs/ea8a5ce3-dccb-49c7-9560-fc4dbb07b99a?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": ".312",
  "substance": "BENZALKONIUM CHLORIDE",
  "productndc": "68062-2219",
  "dosage_form": "SOLUTION",
  "dea_schedule": null,
  "strength_unit": "g/240mL",
  "application_number": "M003",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about benzalkonium chloride.

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.