Is Benoxinate registered with the SFDA?

The SFDA human drug list (edition 4-2026, as published by the Council of Health Insurance) lists 0 valid registrations of Benoxinate.

Is Benoxinate approved by the US FDA?

Drugs@FDA lists 1 application product line for Benoxinate, including BENOXINATE HYDROCHLORIDE (Discontinued).

Active substance

Benoxinate

SFDA 1
US FDA 1

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade name	Strength	Form · route	Pack	Public price	Type	Company	Status
BENOXINATE 0.4% THILO	0.4 %	Eye drops · Ophthalmic use	1 Bottle	SAR 10.90	NCE · Prescription	DR. THILO LABORATORIES	Withdrawn by MAH · Not Marketed

US FDA United States — FDA approvals (Drugs@FDA)

Product	Strength	Form · route	Applicant	Status	First approved
BENOXINATE HYDROCHLORIDE	0.4%	solution/drops · ophthalmic	SOLA BARNES HIND	Discontinued	14 Jan 1975

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.