Ibuprom Ultramax 600 mg painkiller 10 tab.

19,99 

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Returns & Exchanges
  • Return Window: 30 days from delivery for refunds or exchanges.
  • Eligibility: Items must be unused and in original packaging.
  • Process: Contact us to initiate a return. Refunds processed within 5-7 days after receiving the return.
  • Exclusions: Perishables and personalized items cannot be returned.

Description

Ibuprom Ultramax 600 mg painkiller 10 tab.

Ibuprom Ultramax 600mg

10 tablets

Producer

USP HEALTH SP. Z OO

For occasional, short-term use in adults for acute, moderate pain of various origins:

  • headaches (including migraines),
  • toothache,
  • muscle and bone pain (including back pain),
  • post-traumatic and post-operative pain, including pain related to dental procedures,
  • neuralgia,
  • painful menstruation

Dosage

The recommended dose is 600 mg of ibuprofen (1 tablet) once. If necessary, a single dose of 600 mg (1 tablet) can be repeated, maintaining an interval of 6-8 hours. The maximum daily dose, without consulting a doctor, should not exceed 1200 mg (2 tablets).

Composition

The active substance is ibuprofen. Each coated tablet contains 600 mg of ibuprofen.

The other ingredients are: tablet core: hypromellose 2910 (6mPas), croscarmellose sodium, lactose monohydrate, microcrystalline cellulose, pregelatinized maize starch, colloidal anhydrous silica and magnesium stearate; tablet coating: hypromellose 2910 (6mPas), talc and propylene glycol.

Contraindications

When not to use IBUPROM ULTRAMAX:

  • if you are allergic to ibuprofen, other non-steroidal anti-inflammatory drugs (NSAIDs) or any of the other ingredients of this medicine (listed in section 6), – if you have ever had shortness of breath, bronchial asthma, hay fever, swelling or hives after taking acetylsalicylic acid or other similar painkillers (NSAIDs),
  • if you have severe heart failure,
  • if you have severe liver or kidney problems, – if you have unexplained blood formation disorders,
  • if you have brain bleeding or other active bleeding,
  • if you have ever had bleeding or perforation of your stomach or intestines after taking NSAIDs,
  • if you have or have had recurrent gastric and/or duodenal ulcers or gastrointestinal bleeding (at least two confirmed episodes of ulceration or bleeding),
  • if you have severe dehydration (caused by vomiting, diarrhea or insufficient fluid intake),
  • if the patient is in the last trimester of pregnancy,
  • under 18 years of age.

Responsible entity

USP HEALTH SP. Z OO

Poleczki Street 35,

02-822 Warsaw

Before use, read the leaflet, which contains indications, contraindications, data on adverse effects and dosage, and information on the use of the medicinal product, or consult a doctor or pharmacist, as any drug used improperly may threaten your life or health.

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