Is Similasan AG FDA approved?

Similasan AG holds 1 FDA-registered establishment in Switzerland. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are Similasan AG's drugs manufactured?

The FDA register lists Jonen. Registered operations: labelling, finished drug manufacture, repackaging.

What drugs does Similasan AG make?

7 products are listed under Similasan AG in the openFDA NDC Directory, most often as solution/ drops; solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Similasan AG

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 7
Labeller names: 2
Live patents: 0
Countries: 1
Base: Switzerland

Authorisation

Registered operations

Labelling1Finished drug manufacture1Repackaging1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Similasan AG	Chriesiweg 6, Jonen, Aargau 8916, Switzerland (CHE)	Labelling, Finished drug manufacture, Repackaging	1000110034481545754

Catalogue

Drug listings by form and route

7 active NDC listings: 7 human otc drug. By marketing category: UNAPPROVED HOMEOPATHIC 4, OTC MONOGRAPH DRUG 3.

Dosage form	NDCs
solution/ drops	4
solution	3

Route	NDCs
auricular (otic)	4
ophthalmic	3

Labeller name on the listing	NDCs
similasan corporation	6
similasan ag	1

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Complete Eye Relief Sterile Lubricant Eye Drops	hydroxyethyl cellulose	solution/ drops, ophthalmic	59262-805OTC MONOGRAPH DRUG
Dry Eye Relief Sterile Lubricant Eye Drops	glycerin	solution/ drops, ophthalmic	59262-803OTC MONOGRAPH DRUG
Ear Ringing Remedy	ALLYLTHIOUREA, ARNICA MONTANA FLOWER, CALCIUM SULFIDE, ERIODICTYON CALIFORNICUM LEAF, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, QUININE SULFATE, SILICA DIMETHYL SILYLATE	solution, auricular (otic)	59262-275UNAPPROVED HOMEOPATHIC
Ear Wax Relief	causticum, graphite, lachesis muta venom and lycopodium clavatum spore	solution, auricular (otic)	59262-272UNAPPROVED HOMEOPATHIC
Earache Relief	Chamomilla and Mercurius Solubilis and Sulphur	solution, auricular (otic)	53799-277UNAPPROVED HOMEOPATHIC
Irritated Eye Relief Sterile Lubricant Eye Drops	hydroxyethyl cellulose	solution/ drops, ophthalmic	59262-804OTC MONOGRAPH DRUG
Similasan Earache Relief	CHAMOMILE, MERCURIUS SOLUBILIS, SULFUR	solution/ drops, auricular (otic)	59262-271UNAPPROVED HOMEOPATHIC

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MICRO-SPHERE SA1 site · 4 NDC
Corden Pharma Fribourg SA1 site · 3 NDC

Enquiry

Common questions

Is Similasan AG FDA approved?: Similasan AG holds 1 FDA-registered establishment in Switzerland. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Similasan AG's drugs manufactured?: The FDA register lists Jonen. Registered operations: labelling, finished drug manufacture, repackaging.
What drugs does Similasan AG make?: 7 products are listed under Similasan AG in the openFDA NDC Directory, most often as solution/ drops; solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.