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United States· US:0065-1530_303d12ca-c965-4ba2-9723-6162f86fa351

Systane COMPLETE PF

A medicinal product containing propylene glycol, registered in United States by Alcon Laboratories, Inc..

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…normalisedSystane COMPLETE PFATC—REGISTER NO.US:0065-1530_303d12ca…PACKS LISTED4CHECKEDSeptember 27, 2026

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
PROPYLENE GLYCOL
Manufacturer
Alcon Laboratories, Inc.
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 · 4

  • ndc11
    0065153001
    5 VIAL, SINGLE-DOSE in 1 CARTON (0065-1530-01) / .5 mL in 1 VIAL, SINGLE-DOSE
  • ndc11
    0065153004
    30 VIAL, SINGLE-DOSE in 1 CARTON (0065-1530-04) / .5 mL in 1 VIAL, SINGLE-DOSE
  • ndc11
    0065-1530-01
  • ndc11
    0065-1530-04

Regulatory notes

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

Same medicine, other countries

Propylene glycol in 9 other countries

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

All propylene glycol products

Authorised across Europe · EMA

The same active substance is authorised in 7 EEA countries. Names it is sold under:

  • Germany · Propylenglycol Smartpractice Europe
  • Finland · Oviderm
  • United Kingdom (Northern Ireland) · Methadose
  • Iceland · Oviderm
  • Norway · Oviderm
  • Poland · Oviderm
  • Sweden · Oviderm, Propyderm

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/02efb940-0324-4401-a072-f7dc5344f53d
GET /v1/drugs/02efb940-0324-4401-a072-f7dc5344f53d?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": "OPHTHALMIC",
  "source": "ndc",
  "strength": ".06",
  "substance": "PROPYLENE GLYCOL",
  "productndc": "0065-1530",
  "dosage_form": "EMULSION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG"
}

See everything about propylene glycol.

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.