Actimol 500mg Tablet

Actimol 500mg Tablet is a film-coated oral tablet classified as a paracetamol analgesic and antipyretic. Its formulation contains Paracetamol 500 mg per tablet, with the exact strength or quantitative composition to be confirmed from the current product packaging where the batch information does not provide a verified value. The dosage form is designed for the route stated on the label, and the physical characteristics of the product determine how it is prepared, applied or taken. Customers should check the pack before use so that the correct strength, formulation and instructions are matched to the product in hand.

The formulation has a defined pharmaceutical or physical profile rather than being interchangeable with other products that may have a similar brand or general category. Paracetamol acts predominantly within the central nervous system and is associated with inhibition of prostaglandin synthesis pathways involved in pain signalling and temperature regulation. It has comparatively little peripheral anti-inflammatory activity at usual doses. Product handling also matters: application technique, measuring accuracy, contact time and storage conditions can affect appropriate use. Keep the original packaging available so the batch, expiry information and current manufacturer instructions can be checked whenever necessary.

Swallow the tablet with water. It may be taken with or without food. Check other medicines for paracetamol or acetaminophen before taking another product, because combining products can unintentionally increase the total daily dose.

Adults and adolescents aged 12 years and above: follow the product label, commonly 1–2 tablets per dose at the stated interval. Do not exceed 8 tablets (4,000 mg) in 24 hours unless a healthcare professional has specifically advised otherwise. Lower limits may be appropriate for people with liver disease, low body weight, heavy alcohol use or other risk factors.

Store below the temperature stated on the packaging, protected from moisture and direct heat. Keep the tablets in the original blister or container and out of children’s reach.

• Common: Mild local irritation, redness, itching or transient sensitivity may occur, particularly with topical preparations.
• Common: Mild transient discomfort at the application site or sensitivity can occur depending on the formulation.
• Serious: Stop use and seek urgent medical attention for facial or throat swelling, difficulty breathing, widespread blistering rash, severe dizziness or other signs of a serious allergic reaction.

• Known allergy or hypersensitivity to any ingredient in the product.
• Any condition specifically listed as a contraindication on the current package or approved product information.

• Check every other pain, cold or flu medicine for paracetamol or acetaminophen to avoid duplicate dosing.
• Regular heavy alcohol use or medicines that affect the liver should be discussed with a pharmacist or doctor.
• No food interaction is expected to be clinically important at usual doses, but follow the product label.

• Read the current label before the first use and check the strength or formulation.
• Use the measuring device supplied with liquid medicines instead of a household spoon.
• Wash hands before and after topical application unless the hands are the treated area.
• Keep the original packaging so expiry, batch and ingredient information remain available.
• Do not share medicines, applicators or single-use topical products with another person.
• Ask a pharmacist if you are pregnant, breastfeeding, caring for a child, taking regular medicines or unsure about the correct dose.

Precautions: Do not combine with another paracetamol-containing product unless the total dose has been checked. Seek urgent medical advice after an overdose even if the person feels well because serious liver injury can initially have few symptoms.

When to See a Doctor or Pharmacist: Seek medical or dental assessment for severe, persistent, rapidly worsening or unexplained symptoms, or whenever the product is not producing the expected response within the labelled period.