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Solaraze® 3% Gel – patient leaflet, side effects, dosage

Updated:
Key facts
Status:
Prescription only (POM)
Medicine strength:
3%
Contains active substance:
ATC code:

Patient leaflet - Solaraze 3% gel,Diclofenac Sodium 3% w/w gel

1. WHAT SOLARAZE IS AND WHAT IT IS USED FOR

Solaraze is a non-steroidal anti-inflammatory dermatological gel. When applied to the skin, Solaraze gel is used to treat a skin problem known as actinic or solar keratosis that is caused by long-term sun exposure.

2. BEFORE YOU USE SOLARAZE

Do not use Solaraze

  • If you are allergic to diclofenac or any of the ingredients in Solaraze.
  • If you have had an allergic reaction such as skin rash (nettle rash), breathing difficulties (wheezing) or runny nose (allergic rhinitis) after taking aspirin or any other non-steroidal anti-inflammatory agents.
  • If you are in the final 3 months of your pregnancy.

Take special care with Solaraze

  • The possibility of systemic side effects from application of Solaraze cannot be excluded if the product is used on large areas of skin and over a prolonged period. Consult your doctor if:

    • you have, or have had in the past, a stomach ulcer or bleeding from the stomach.
    • you have heart, liver or kidney problems.
    • you have any type of bleeding disorder or bruise very easily.
  • Avoid sun exposure, including tanning salons, when using Solaraze. If skin reactions occur, discontinue use.
  • Do not apply to skin wounds, infected skin or dermatitis.
  • Do not allow Solaraze to come into contact with your eyes or the inside of your nose or mouth and do not swallow it. If Solaraze has accidentally been swallowed, consult a doctor immediately.
  • Discontinue Solaraze and consult your doctor if you develop a wide-spread skin rash.
  • After applying products containing diclofenac on the skin you can use a permeable (non-occlusive) bandage. Do not use an airtight occlusive dressing.

Pregnancy/Breastfeeding

Speak to your doctor if you are, or could be pregnant. Solaraze should be used with caution during the first six months of pregnancy but must not be used during the last three months of pregnancy.

Consult your doctor if you are breastfeeding. Solaraze can be used whilst breastfeeding with caution but should not be used on the breasts. If you are pregnant, trying to get pregnant, or breastfeeding, and your doctor considers treatment appropriate, Solaraze must not be applied to an area of the skin larger than about a third of your body and must not be used for longer than three weeks. Ask your doctor or pharmacist for advice before taking or using any medicine.

3. HOW TO USE SOLARAZE

  • Solaraze is not suitable for children.
  • Use the gel as directed by your doctor.
  • Pierce the aluminium membrane across the tube opening with the cap before using.
  • Gently smooth a small amount of gel onto the skin over the area to be treated. The amount of gel needed will vary depending upon the size of the area to be treated. Usually 0.5 grams of gel (about the size of a pea) will be enough for one area (5cm x 5cm) but not more than 8 grams should be used per day.
  • You can apply Solaraze twice daily unless your doctor tells you differently. You may notice a slight cooling effect when you smooth the gel onto your skin.
  • The usual period of treatment is 60-90 days. Maximum effect has been seen with treatment times closer to 90 days. Complete healing may not occur for up to a month after treatment has stopped.
  • Wash your hands after applying the gel, unless your hands are being treated.

    If you use more Solaraze than you should

    Remove the excess gel by washing with water.

    If you forget to use Solaraze

    Continue to apply as directed but do not apply twice as much to make up for the missed application.

4. POSSIBLE SIDE EFFECTS

Like all medicines, Solaraze can have side effects although not everybody gets them.

If you have any of the following side effects, stop using Solaraze and contact your doctor as soon as possible:

Skin rash (nettle rash); breathing difficulties (wheezing); swelling of the face; runny nose (allergic rhinitis). These symptoms indicate that you may be allergic to Solaraze.

If any of the following common side effects are severe or last for more than a few days you should stop using Solaraze and contact your doctor: itching, rash, skin redness, inflammation, contact dermatitis, pain and blistering.

Other common side effects: (occur in between 1 and 10 out of every 100 patients)

Irritation or tingling at the site of treatment, conjunctivitis, allergy, a painful sensation when the skin is touched, pins and needles, muscle stiffness, dermatitis, eczema, dry skin, swelling, rash (including scaly or blistering), sagging of the skin, and skin ulcer.

Uncommon side effects: (occur in between 1 and 10 out of every 1,000 patients)

Eye pain, weeping/dry eyes, pain in the abdomen, diarrhoea, feeling sick, hair loss, facial swelling, excessive bleeding or oily skin, a measles-like rash.

Rare side effects: (occur in between 1 and 10 out of every 10,000 patients) Dermatitis with large blisters.

Very rare side effects: (occur in fewer than 1 in 10,000 patients) Bleeding from your stomach, problems with your kidneys, breathing difficulties (asthma), infected skin rash, skin sensitivity to sunlight. Temporary hair discolouration at the application site has been reported. This is usually reversed on stopping treatment.

Reporting of side effects

If you get any side effects, talk to your doctor, pharmacist, or nurse. 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. By reporting side effects, you can help provide more information on the safety of this medicine.

5. HOW TO STORE SOLARAZE

Keep Solaraze out of the sight and reach of children.

Do not use after the expiry date on the tube and carton. The date refers to the last date of that month.

Do not store above 25°C.

Shelf life after opening: 6 months.

If your gel becomes discoloured or shows any other signs of deterioration, please ask your doctor or pharmacist before using your medicine. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.

6. FURTHER INFORMATION

What Solaraze contains

  • Each gram of gel contains the equivalent of 30mg diclofenac sodium (the active substance).
  • The gel also contains sodium hyaluronate, benzyl alcohol, macrogol monomethyl ether 350 and purified water.

What Solaraze looks like and contents of the pack

Solaraze gel is a clear, transparent, colourless or pale yellow gel packed in tubes containing 25 grams, 2 x 25 grams or 4 x 25 grams of product.

MANUFACTURER AND PRODUCT LICENCE HOLDER Manufactured by Almirall Hermal GmbH, Scholtzstrasse 3, D-21465 Reinbek, Germany. Procured from within the EU by Product Licence holder Star Pharmaceuticals Ltd., 5 Sandridge Close, Harrow, Middesex, HA1 1XD. Repackaged by Servipharm Ltd.

Leaflet revision and issue date (Ref) 29.04.16[3]

Solaraze is a trademark of Almirall S.A.

2850

29.04.16[3]

POM PL 20636/2850

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk)

Last revision stated in the text: 29 April 2016

What the sections and the side effect frequencies mean: How to read a patient leaflet

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

Facts about Solaraze 3% gel,Diclofenac Sodium 3% w/w gel

What these facts mean

Prescription needed?? Yes, prescription-only medicine (POM)
Active substance? Diclofenac sodium
Strength? 3%
Is it available?? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Drug group (ATC)?
  1. M Musculo-skeletal system drugs
    1. M02 Topical products for joint and muscular pain
      1. M02A Topical products for joint and muscular pain
        1. M02AA Antiinflammatory preparations, non-steroids for topical use
          1. M02AA15 diclofenac

Sources: the NHS Dictionary of Medicines and Devices (dm+d), release 11.1.0 of 9 November 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.