Precoxin®
Precoxin is a 10% spray solution containing the active substance lidocaine hydrochloride.
Prescription only. This page provides marketing authorisation particulars.
This is a prescription medicinal product authorised in the name of Aymed İlaç Sanayi. It is a white, lavender-scented spray solution containing 115.5 mg of lidocaine hydrochloride, equivalent to 100 mg of lidocaine, per 1 mL.
According to the SmPC, the product is supplied in a 40 mL aluminium tube with a polypropylene cap. The SmPC and patient leaflet contain the authoritative information on use.
- Product name
- Precoxin® 10% spray solution
- Product category
- Medicinal product for human use
- Active substance
- Lidocaine hydrochloride
- Pharmaceutical form
- Spray solution
- Strength
- 10%
- Pack
- 40 mL aluminium tube
- ATC code
- N01BB02
- Marketing authorisation number
- 2017/8
- Date of first authorisation
- 12.01.2017
- Marketing authorisation holder
- Aymed İlaç Sanayi
- Supply status
- Prescription only
Composition and pharmaceutical characteristics
The information below is taken from the composition, pharmaceutical form and pharmaceutical particulars sections of the Summary of Product Characteristics.
- Composition
- Each 1 mL contains 115.5 mg of lidocaine hydrochloride, equivalent to 100 mg of lidocaine.
- Description of pharmaceutical form
- White, lavender-scented spray solution.
- Excipients
- Polyethylene glycol 400, propylene glycol, chlorhexidine digluconate (20% w/v), lavender essence, purified water
- Shelf life
- 24 months
- Storage
- Store at room temperature below 25 °C.
Product documents
The Summary of Product Characteristics (SmPC) is intended for healthcare professionals; the patient information leaflet provides information for patients. This website asks you to confirm that you are a healthcare professional before accessing the Precoxin documents.
Translations are provided for information. The Turkish SmPC and patient leaflet contain the authoritative product information.
Frequently asked questions
Is Precoxin prescription only?
Yes. Precoxin is a medicinal product for human use and is supplied on prescription. A physician decides whether it should be used.
What is the active substance in Precoxin?
The active substance is lidocaine hydrochloride. According to the SmPC, 1 mL contains 115.5 mg of lidocaine hydrochloride, equivalent to 100 mg of lidocaine.
How is Precoxin packaged?
According to the SmPC, the product is supplied in a 40 mL aluminium tube with a polypropylene cap.
How can I access the Precoxin SmPC and patient leaflet?
The documents are in the Product documents section on this page. The SmPC is for healthcare professionals and the leaflet is for patients. Access on this website requires confirmation of healthcare professional status.
Who holds the marketing authorisation for Precoxin?
The marketing authorisation holder is Aymed İlaç Sanayi. The authorisation number is 2017/8 and the date of first authorisation is 12.01.2017.
The particulars on this page are taken from the Summary of Product Characteristics; authoritative information is contained in the SmPC and patient leaflet. Consult your physician about your medicine and your pharmacist about its use. Other medicinal products from Aymed İlaç Sanayi are listed on the Prescription medicines page.