Carbomer-980 (Viscotears)
What to know about Carbomer-980 — also sold as Viscotears, PAA, Optifresh eye gel, Viscotears Gel PF: uses, side effects, interactions, and safety considerations for people taking it or caring for someone who is.
Carbomer-980 (brand names: Viscotears, PAA, Optifresh eye gel, Viscotears Gel PF) is classified as Minimal risk by AllMeds. It is a S2 medication under the TGA in Australia. Topical ophthalmic lubricant with no systemic absorption or workplace impairment risk.
Key Takeaways
- TGA Schedule: S2 in Australia
- Risk level: Minimal (0 points)
- PBS listed: Subsidised under the Australian Pharmaceutical Benefits Scheme
Scheduling and Classification
| Jurisdiction | Classification | Status |
|---|---|---|
| Australia (TGA) | S2 | PBS listed |
Risk Profile
Topical ophthalmic lubricant with no systemic absorption or workplace impairment risk.
How Carbomer-980 is regulated
Carbomer-980 is overseen by medicines regulators in each country. The rules below explain how it's scheduled, what oversight applies, and what to discuss with your doctor or pharmacist before starting, changing, or stopping this medication.
Australia TGA / PBS / State Schemes
Classified as S2 under the Therapeutic Goods Administration (TGA).
Listed on the Pharmaceutical Benefits Scheme (PBS) for subsidised prescribing.
Check this medication against your full medication list
Run a full risk assessment including Carbomer-980 interactions and compliance checks.
Allmeds AI Pharmacist scans interactions, schedules, and risk flags across your entire medication profile in minutes. Free for individuals; team plans for case managers, insurers, and schemes.
Important: This page is general health information, not personal medical advice. If you have questions about your medication — including starting it, stopping it, changing the dose, or combining it with something else — speak with your doctor or pharmacist. For an emergency or suspected overdose, call your local emergency number or poison information service immediately. Information is drawn from regulator and clinical guideline sources (TGA, FDA, MHRA, NICE, PBS, CDC); see our methodology for details.