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Fluoritop LF 2800 PPM Fluoride toothpaste – patient leaflet, side effects, dosage

Last updated: · Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) Details

Contains active substance:
ATC code:
Similar medicines:

Sources: Original (products.mhra.gov.uk) · About this document

Patient leaflet - Fluoritop LF 2800 PPM Fluoride toothpaste

1. WHAT FLUORITOP TOOTHPASTE IS AND WHAT IT IS USED FOR

Fluoritop toothpaste contains fluoride as sodium salt, which belongs to a group of medicines called caries preventing agents.

This toothpaste is used for the treatment of tooth decay (dental caries) of the tooth crown and root, in adolescents and children over 10 years. Do not swallow. You must talk to a doctor if you do not feel better or if you feel worse.

2. WHAT YOU NEED TO KNOW BEFORE YOU USE FLUORITOP TOOTHPASTES

Do not use Fluoritop toothpastes;

  • If you are allergic to sodium fluoride or any of the other ingredients of this medicine (listed in section 6)

  • If you are a child less than 10 years old.

    Warnings and precautions

    Talk to your doctor, dentist or pharmacist before using Fluoritop toothpastes;

    Fluoritop Toothpaste has high fluoride content. In order to prevent build up of fluoride, your total intake must be assessed before using this Fluoritop toothpaste.

    Children and adolescents

    Fluoritop Toothpaste is not intended for use by children aged less than 10 years.

    Other medicines and Fluoritop toothpaste

    No interactions with other medicines are known.

    Tell your doctor, dentist or pharmacist if you are taking or using, or have recently taken or used, or might take or use any other medicines, including medicines obtained without a prescription.

    Fluoritop Toothpaste with food and drink

    Fluoridated water and salt should be avoided while using this toothpaste. Food and drink, if taken immediately after brushing your teeth, may reduce the amount of tooth remineralisation that occurs. You should therefore brush your teeth with Fluoritop Toothpaste after meals.

    Pregnancy, breast feeding and fertility

    There is no adequate data from the use of fluoride toothpaste in pregnant women. If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor, dentist, or pharmacist for advice before taking this medicine.

    Important information about some of the ingredients of Fluoritop toothpaste

    If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicinal product.

    This toothpaste contains Sodium Benzoate. Sodium Benzoate is a mild irritant to the skin, eyes and mucous membrane.

3. HOW TO USE FLUORITOP TOOTHPASTE

Always take this medicine exactly as your doctor, dentist or pharmacist has told you or as described in this leaflet. Check with your doctor, dentist or pharmacist if you are not sure.

Fluoritop toothpaste is only for use by adolescents and children over 10 years old:

Title: Fluoritop LF 2800 PPM Size: 170x190mm

Colours: Black (process)

Use twice a day; morning and evening instead of your normal toothpaste.

The usual dosage is to apply a 1 cm ribbon of paste across the head of a toothbrush and brush the teeth thoroughly for one minute morning and evening. Spit out after use; for best results do not drink or rinse for 30 minutes

Use in children and adolescents:

Fluoritop toothpaste is not for use by children aged less than 10 years.

If you use more toothpaste than you should or if you have swallowed the toothpaste:

Consult your doctor immediately, if you swallowed a large amount of toothpaste by mistake, and if you experience digestive problems such as being sick, diarrhoea, vomiting and pain in the stomach or abdomen as you may require treatment. Please take this leaflet with you.

If you constantly swallow too much of the toothpaste over several months, or years, you may get stained or speckled appearance of tooth enamel, and enamel fragility (dental fluorosis), or increased bone density, osteosclerosis (bone fluorosis).

If you forget to take Fluoritop toothpaste:

Use as soon as you remember, but do not use a double dose to make up for a missed dose.

If you have any further questions on the use of this medicine, ask your doctor, dentist or pharmacist.

4. POSSIBLE SIDE EFFECTS

Like all medicines, this medicine can cause side effects although not everybody gets them.

In some rare cases (less than 1 in 1,000 users) allergic (hypersensitivity) reactions can occur, such as rash, itching, swelling, and redness. Burning oral sensation has also been reported.

Reporting of side effects

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google play or Apple App Store.

By reporting side effects you can help provide more information on the safety of this medicine.

5. HOW TO STORE FLUORITOP TOOTHPASTE

Keep this medicine out of the sight and reach of children.

Replace the tube cap after use. This medicinal product does not require any special storage conditions.

Do not use Fluoritop toothpaste after the expiry date which is stated on the tube and carton after EXP. The expiry date refers to the last day of the month. Discard 6 months after opening.

Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

6. CONTENTS OF THE PACK AND OTHER INFORMATION

What Fluoritop toothpaste contains

Each 1gm of toothpaste contains 2.8mg fluoride (as sodium fluoride), which is 2800 ppm fluoride.

The other ingredients are; glycerol E422, sorbitol liquid (non-crystallising) E420, carmellose sodium, sodium saccharine, sodium benzoate E211, macrogols 600, dental type silicas, titanium dioxide E171, sodium laurilsulfate, flavour mint sc and purified water.

What Fluoritop toothpaste looks like and contents of the pack

Fluoritop toothpaste is a white homogenous paste and available in a 75ml of laminated tube.

Enclosed in an outer carton.

Marketing Authorisation Holder and Manufacturer

Marketing Authorisation Holder

RxFarma, Colonial Way, Watford, Hertfordshire, WD24 4YR.

Manufacturer

Rx Farma Limited, Unit 3, Colonial Way,

Watford, Hertfordshire, WD24 4YR

If you would like this leaflet in different format or want to report any side effects please contact marketing authorisation holder listed above.

This leaflet was last revised in July 2025

Title: Fluoritop HF 2800 PPM

Size: 170x190mm

Colours: Black (process)

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 36722/0076

Last revision stated in the text: July 2025 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Fluoritop LF 2800 PPM Fluoride toothpaste

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Sodium fluoride
Pharmaceutical form A white homogenous paste.
For dental use.
Excipients Glycerol E422, Sorbitol, liquid (non-crystallising) E420, Carmellose Sodium, Sodium Saccharine, Sodium Benzoate E211, Macrogols 600, Dental type silicas, Titanium Dioxide E171, Sodium laurilsulfate, Flavour mint SC, Purified water
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 3 years unopened
6 months after opening
Storage This product requires no special storage conditions.
Drug group (ATC)
  1. A Alimentary tract and metabolism drugs
    1. A01 Stomatological preparations
      1. A01A Stomatological preparations
        1. A01AA Caries prophylactic agents
          1. A01AA01 sodium fluoride
Marketing authorisation PL 36722/0076 (first authorised 8 April 2025)
Marketing authorisation holder Special Concept Development (UK) Limited T/A Rx Farma.

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.2.0 of 19 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.