United States· US:0065-1433_f81c8282-0871-46fb-8124-83666457a4f2
Systane Balance
A medicinal product containing propylene glycol, registered in United States by Alcon Laboratories, Inc..
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
- 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 · 6
- ndc1100651433021 BOTTLE, DROPPER in 1 CARTON (0065-1433-02) / 10 mL in 1 BOTTLE, DROPPER
- ndc1100651433072 BOTTLE, DROPPER in 1 CARTON (0065-1433-07) / 10 mL in 1 BOTTLE, DROPPER
- ndc1100651433111 BOTTLE, DROPPER in 1 CARTON (0065-1433-11) / 1.5 mL in 1 BOTTLE, DROPPER
- ndc110065-1433-02
- ndc110065-1433-07
- ndc110065-1433-11
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.
- United KingdomAserbine solutionMercury Pharma Group Ltd
- SwedenOviderm 250 mg/g KrämGalenica AB
- CanadaPROPYLENE GLYCOLPARTNAR ANIMAL HEALTH INC.
- IcelandOvidermGalenica AB
- Japanプロピレングリコール
- NorwayOvidermGalenica AB
- PolandOvidermReig Jofre Sp. z o.o.
- FinlandOvidermGalenica AB
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/0b95b1f4-787e-424f-9501-0ddccb01c4b9 GET /v1/drugs/0b95b1f4-787e-424f-9501-0ddccb01c4b9?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": "0065-1433",
"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.