Motrin Junior Strength

The recommended adult dose of Motrin Junior Strength (Ibuprofen) is 200 mg to 400 mg every 6 to 8 hours as required. Extended-release tablets should be taken as 1 tablet (600 mg) every 12 hours. The maximum daily dose is 1,200 mg. Motrin Junior Strength (Ibuprofen) available without a prescription should not be taken for more than 3 consecutive days for a fever or 5 consecutive days for pain unless advised by your doctor. The lowest dose for the shortest period of time should be used to reduce the risk of side effects.

The dose of Motrin Junior Strength (Ibuprofen) for children is based on body weight and age. Ask your doctor or pharmacist for specific dosing information. Children should not take more than 40 mg per kilogram of body weight each day.

Use an oral syringe to measure each dose of the liquid, as it gives a more accurate measurement than household teaspoons.

Take Motrin Junior Strength (Ibuprofen) with food or milk to minimize side effects such as heartburn and stomach upset. The suspension form should be shaken well before using.

Many things can affect the dose of a medication that a person needs, such as body weight, other medical conditions, and other medications. If your doctor has recommended a dose different from the ones listed here, do not change the way that you are taking the medication without consulting your doctor.

It is important to take Motrin Junior Strength (Ibuprofen) exactly as prescribed by your doctor. If you miss a dose, take it as soon as possible and continue with your regular schedule. If it is almost time for your next dose, skip the missed dose and continue with your regular dosing schedule. Do not take a double dose to make up for a missed one. If you are not sure what to do after missing a dose, contact your doctor or pharmacist for advice.

Store Motrin Junior Strength (Ibuprofen) at room temperature, protect it from heat and moisture, and keep it out of the reach of children.

Do not dispose of medications in wastewater (e.g. down the sink or in the toilet) or in household garbage. Ask your pharmacist how to dispose of medications that are no longer needed or have expired.

Motrin IB

Caplet

Motrin Caplets is no longer being manufactured for sale in Canada. For brands that may still be available, search under Motrin Junior Strength (Ibuprofen). This article is being kept available for reference purposes only. If you are using Motrin Junior Strength (Ibuprofen), speak with your doctor or pharmacist for information about your treatment options.

Tablet

200 mg
Each white, sweet-coated, biconvex tablet, with "Motrin IB" printed in black ink, contains 200 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: colloidal silicon dioxide, cornstarch, hypromellose, iron oxide black, polyethylene glycol, pregelatinized starch, propylene glycol, sodium cyclamate, sodium starch glycolate, stearic acid, and titanium dioxide. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, paraben, sulfite, or tartrazine.

300 mg
Each solid, light orange, round, biconvex, sweet-coated tablet, with "MOTRIN 300 mg" printed in black ink, contains 300 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: carnauba wax, colloidal silicon dioxide, cornstarch, FD&C Yellow No. 6, hypromellose, iron oxide black, polydextrose, polyethylene glycol, propylene glycol, sodium cyclamate, sodium starch glycolate, stearic acid, and titanium dioxide. Motrin Junior Strength (Ibuprofen) does not contain gluten or lactose.

400 mg
Each solid, orange, round, biconvex, sweet-coated tablet, with "MOTRIN 400 mg" printed in black ink, contains 400 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: carnauba wax, colloidal silicon dioxide, cornstarch, FD&C Yellow No. 6, hypromellose, iron oxide black, polydextrose, polyethylene glycol, propylene glycol, sodium cyclamate, sodium starch glycolate, stearic acid, and titanium dioxide. Motrin Junior Strength (Ibuprofen) does not contain gluten or lactose.

Motrin IB Gelcaps

Motrin IB Gelcaps is no longer being manufactured for sale in Canada. For brands that may still be available, search under Motrin Junior Strength (Ibuprofen). This article is being kept available for reference purposes only. If you are using Motrin Junior Strength (Ibuprofen), speak with your doctor or pharmacist for information about your treatment options.

Motrin IB Liquid Gels
Each capsule of clear, colourless-to-pale yellow solution in a clear, green oblong gelatin shell, printed with the "200" logo in white ink, contains 200 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients:castor oil, FD&C Green No. 3, gelatin, PEG-40 hydrogenated castor oil, povidone, purified water, sorbitan, sorbitol, and titanium dioxide.

Super Strength Motrin IB Liquid Gels

Super Strength Motrin IB Liquid Gels is no longer being manufactured for sale in Canada. For brands that may still be available, search under Motrin Junior Strength (Ibuprofen). This article is being kept available for reference purposes only. If you are using Motrin Junior Strength (Ibuprofen), speak with your doctor or pharmacist for information about your treatment options.

Super Strength Motrin IB Liquid Gels Capsule
Each capsule of clear, colourless-to-pale yellow solution in a clear oval soft gelatin shell, printed with the "M400" logo in black ink, contains 400 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: gelatin, pharmaceutical ink, polyethylene glycol, potassium hydroxide, propylene glycol, purified water, and sorbitol.

Children's Chewable Tablets

Grape
Each round, purple tablet with a grape odour, debossed with ''MO'' and ''50'' on one side and scored on the other side, contains 50 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: acesulfame potassium, aspartame, citric acid, D&C Red No. 7 Calcium Lake, D&C Red No. 30 Aluminum Lake, FD&C Blue No.1 Aluminum Lake, flavour, fumaric acid, hydroxyethyl cellulose, hypromellose, magnesium stearate, mannitol, microcrystalline cellulose, povidone, sodium lauryl sulfate, and sodium starch glycolate. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, sucrose, sulfite, or tartrazine.

Orange
Each round, light orange tablet with an orange odour, debossed with "MO" and "50" on one side and scored on the other side, contains 50 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: acesulfame potassium, aspartame, citric acid, FD&C Yellow No. 6 Aluminum Lake, flavour, fumaric acid, hydroxyethyl cellulose, hypromellose, magnesium stearate, mannitol, microcrystalline cellulose, povidone, sodium lauryl sulfate, and sodium starch glycolate. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, sucrose, sulfite, or tartrazine.

Children's Suspension Liquid

Berry
Each 5 mL of orange liquid suspension with a distinct berry odour contains 100 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: acesulfame potassium, citric acid, D&C Yellow No. 10, FD&C Red No. 40, flavour, glycerin, hydroxypropyl distarch phosphate, polysorbate 80, purified water, sodium benzoate, sucrose, and xanthan gum. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, sulfite, or tartrazine.

Bubblegum
Each 5 mL of pink liquid suspension with a distinct bubblegum odour contains 100 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: acesulfame potassium, citric acid, FD&C Red No. 40, flavour, glycerin, hydroxypropyl distarch phosphate, polysorbate 80, purified water, sodium benzoate, sucrose, and xanthan gum. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, sulfite, or tartrazine.

Dye-Free Berry
Each 5 mL of white liquid suspension with a distinct berry odour contains 100 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: acesulfame potassium, citric acid, flavour, glycerin, hydroxypropyl distarch phosphate, polysorbate 80, purified water, sodium benzoate, sucrose, and xanthan gum. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, sulfite, or tartrazine.

Grape
Each 5 mL of purple liquid suspension with a distinct grape odour contains 100 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: acesulfame potassium, citric acid, D&C Red No. 33, FD&C Blue No. 1, FD&C Red No. 40, flavour, glycerin, hydroxypropyl distarch phosphate, polysorbate 80, purified water, sodium benzoate, sucrose, and xanthan gum. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, sulfite, or tartrazine.

Tropical Punch
Each 5 mL of red liquid suspension with a distinct tropical punch odour contains 100 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: acesulfame potassium, citric acid, FD&C Red No. 40, flavor, glycerin, hydroxypropyl distarch phosphate, polysorbate 80, potassium sorbate, purified water, sodium benzoate, sucralose, sucrose, and xanthan gum. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, sulfite, or tartrazine.

Infants Suspension Drops

Berry
Each mL of pink-coloured, berry-flavoured liquid suspension contains 40 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: citric acid, cornstarch, FD&C Red No. 40, flavour, glycerin, polysorbate 80, purified water, sodium benzoate, sorbitol, sucrose, and xanthan gum. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, sulfite, or tartrazine.

Berry Dye-Free
Each mL of white-coloured, berry-flavoured liquid suspension contains 40 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: citric acid, cornstarch, flavour, glycerin, polysorbate 80, purified water, sodium benzoate, sorbitol, sucrose, and xanthan gum. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, sulfite, or tartrazine.

Junior Strength Chewable Tablets

Grape
Each round, purple tablet with a grape odour, debossed with ''MO'' and ''100'' on one side and scored on the other side, contains 100 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: acesulfame potassium, aspartame, citric acid, D&C Red No. 7 Calcium Lake, D&C Red. No. 30 Aluminum Lake, FD&C Blue No. 1 Aluminum Lake, flavour, fumaric acid, hydroxyethyl cellulose, hypromellose, magnesium stearate, mannitol, microcrystalline cellulose, povidone, sodium lauryl sulfate, and sodium starch glycolate. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, sucrose, sulfite, or tartrazine.

Orange
Each round, light orange tablet with an orange odour, debossed with ''MO'' and ''100'' on one side and scored on the other side, contains 100 mg of Motrin Junior Strength (Ibuprofen). Nonmedicinal ingredients: acesulfame potassium, aspartame, citric acid, FD&C Yellow No. 6 Aluminum Lake, flavour, fumaric acid, hydroxyethyl cellulose, hypromellose, magnesium stearate, mannitol, microcrystalline cellulose, povidone, sodium lauryl sulfate, and sodium starch glycolate. Motrin Junior Strength (Ibuprofen) does not contain gluten, lactose, sucrose, sulfite, or tartrazine.

Junior Strength Motrin Caplets

Junior Strength Motrin Caplets is no longer being manufactured for sale in Canada. For brands that may still be available, search under Motrin Junior Strength (Ibuprofen). This article is being kept available for reference purposes only. If you are using Motrin Junior Strength (Ibuprofen), speak with your doctor or pharmacist for information about your treatment options.

Do not use Motrin Junior Strength (Ibuprofen) if you:

• are allergic to Motrin Junior Strength (Ibuprofen) or any ingredients of Motrin Junior Strength (Ibuprofen)
• are allergic to other NSAIDs
• are currently taking other NSAIDs
• are pregnant or breast-feeding
• are dehydrated due to vomiting, Diarrhea, or lack of fluid intake
• have an active peptic ulcer, a history of recurring ulcers, or an active inflammatory disease of the digestive system (such as Crohn's Disease or Ulcerative Colitis)
• have nasal polyps, or have had Asthma, an allergic reaction or allergic-type reaction (e.g., difficulty breathing, wheezing, itchy skin rash, swelling of the face, throat, or tongue) to Asa (acetylsalicylic acid) or any other NSAIDs (nonsteroidal anti-inflammatory drugs; e.g., Ketorolac, Indomethacin, Naproxen)
• have severely reduced kidney function or Kidney Disease
• have severely reduced liver function or liver disease
• have high levels of potassium in the blood
• have systemic Lupus erythematosus
• have severe heart failure
• have inflammatory bowel disease
• are having heart surgery in the near future or have recently had heart surgery

Do not give Motrin Junior Strength (Ibuprofen) to children who have kidney disease or have suffered significant fluid loss.

There may be an interaction between Motrin Junior Strength (Ibuprofen) and any of the following:

• acetylsalicylic acid (ASA)
• alcohol
• Aliskiren
• aminoglycoside antibiotics (e.g., Amikacin, gentamicin, tobramycin)
• angiotensin-converting enzyme (ACE) inhibitors (e.g., Enalapril, Lisinopril, ramipril)
• angiotensin receptor blockers (ARBs; e.g., Candesartan, Irbesartan, Losartan)
• anticoagulants (e.g., Dalteparin, Enoxaparin, heparin, Tinzaparin, warfarin)
• Apixaban
• beta-adrenergic blockers (e.g., Atenolol, Propranolol, Sotalol)
• Bimatoprost
• Bismuth Subsalicylate
• bisphosphonates (e.g., Alendronate, etidronate)
• Celecoxib
• Cholestyramine
• Clopidogrel
• Colestipol
• corticosteroids (e.g., Dexamethasone, Hydrocortisone, Prednisone)
• Cyclosporine
• dabigatran
• Dasatinib
• Deferasirox
• Desmopressin
• Digoxin
• Dipyridamole
• diuretics (e.g., Furosemide, Hydrochlorothiazide, Spironolactone)
• Edoxaban
• Eplerenone
• glucosamine
• Haloperidol
• Hydralazine
• imatinib
• Latanoprost
• lithium
• Mesalamine
• Methotrexate
• multivitamins
• Obinutuzumab
• other non-steroidal anti-inflammatory medications (NSAIDs; e.g., ketorolac, indomethacin, naproxen)
• omega-3 fatty acids
• Pentoxifylline
• Porfimer
• quinolone antibiotics (e.g., ciprofloxacin, Norfloxacin, Ofloxacin)
• Rivaroxaban
• selective serotonin reuptake inhibitors (SSRIs; e.g., Citalopram, Fluoxetine, Paroxetine, Sertraline)
• serotonin/norepinephrine reuptake inhibitors (SNRIs; e.g., Desvenlafaxine, Duloxetine, Venlafaxine)
• sodium phosphates
• Sulfasalazine
• Tacrolimus
• tenofovir
• Ticagrelor
• Ticlopidine
• tipranavir
• tricyclic antidepressants (e.g., Amitriptyline, Clomipramine, Desipramine, Trimipramine)
• vancomycin
• vitamin E
• Voriconazole
• warfarin

If you are taking any of these medications, speak with your doctor or pharmacist. Depending on your specific circumstances, your doctor may want you to:

• stop taking one of the medications,
• change one of the medications to another,
• change how you are taking one or both of the medications, or
• leave everything as is.

An interaction between two medications does not always mean that you must stop taking one of them. Speak to your doctor about how any drug interactions are being managed or should be managed.

Medications other than those listed above may interact with Motrin Junior Strength (Ibuprofen). Tell your doctor or prescriber about all prescription, over-the-counter (non-prescription), and herbal medications you are taking. Also tell them about any supplements you take. Since caffeine, alcohol, the Nicotine from cigarettes, or street drugs can affect the action of many medications, you should let your prescriber know if you use them.

Before you begin using a medication, be sure to inform your doctor of any medical conditions or Allergies you may have, any medications you are taking, whether you are pregnant or breast-feeding, and any other significant facts about your health. These factors may affect how you should use Motrin Junior Strength (Ibuprofen).

HEALTH CANADA ADVISORY

June 8, 2021

Health Canada has issued new information concerning the use of non-steroidal anti-inflammatory drugs (NSAIDs). To read the full Health Canada Advisory, visit Health Canada's web site at www.hc-sc.gc.ca.

A previous advisory on non-steroidal anti-inflammatory drugs (NSAIDs) was issued on October 30, 2020.

Allergy: Some people who are allergic to other anti-inflammatory medications also experience allergic reactions to Motrin Junior Strength (Ibuprofen). Before you take Motrin Junior Strength (Ibuprofen), inform your doctor or pharmacist about any previous adverse reactions you have had to medications, especially ASA or naproxen. Contact your doctor at once if you experience signs of an allergic reaction, such as skin rash, itching, difficulty breathing, or swelling of the face and throat.

Bladder problems: Motrin Junior Strength (Ibuprofen) may cause bladder pain, painful or difficult urination, or increased frequency of urination. If these symptoms occur without an explanation (e.g., infection), stop taking Motrin Junior Strength (Ibuprofen) and contact your doctor.

Blood clotting: Motrin Junior Strength (Ibuprofen) may reduce the ability of the blood to clot. If you are taking anticoagulants (e.g., Warfarin, Heparin) or have Hemophilia or other blood disorders (e.g., low platelets), discuss with your doctor how Motrin Junior Strength (Ibuprofen) may affect your medical condition, how your medical condition may affect the dosing and effectiveness of Motrin Junior Strength (Ibuprofen), and whether any special monitoring is needed.

Blood pressure: Motrin Junior Strength (Ibuprofen) may cause an increase in blood pressure, particularly for people who already have high blood pressure. If you are taking medications for blood pressure or are at risk of developing high blood pressure, discuss with your doctor how Motrin Junior Strength (Ibuprofen) may affect your medical condition, how your medical condition may affect the dosing and effectiveness of Motrin Junior Strength (Ibuprofen), and whether any special monitoring is needed.

Fluid and electrolyte balance: Fluid retention and edema have been reported with use of Motrin Junior Strength (Ibuprofen). Use Motrin Junior Strength (Ibuprofen) with caution if you:

• are recovering from a surgical operation under general anesthesia
• have certain heart conditions (e.g., Congestive Heart Failure)
• have high blood pressure
• have kidney disease or reduced kidney function
• have any other condition that might lead to fluid retention

Gastrointestinal problems: Stomach ulcers, perforation, and bleeding from the stomach have been known to occur during therapy with Motrin Junior Strength (Ibuprofen). These complications can occur at any time and are sometimes severe enough to require immediate medical attention.

The risk of ulcers and bleeding increases for people taking higher doses of Motrin Junior Strength (Ibuprofen) for longer periods of time. Stomach problems are also more likely to occur with alcohol use. Do not drink alcohol while taking Motrin Junior Strength (Ibuprofen).

If you are prone to irritation of the stomach and intestines, particularly if you have had a stomach ulcer, bloody stools, diverticulosis, or other inflammatory disease of the stomach or intestines (such as ulcerative colitis or Crohn's disease), discuss with your doctor how Motrin Junior Strength (Ibuprofen) may affect your medical condition, how your medical condition may affect the dosing and effectiveness of Motrin Junior Strength (Ibuprofen), and whether any special monitoring is needed.

Stop taking the medication and contact your doctor immediately if you experience symptoms or signs suggestive of stomach ulcers or bleeding in the stomach (black, tarry stools). These reactions can occur at any time without warning during treatment.

Heart attack and stroke: High doses of Motrin Junior Strength (Ibuprofen) (2,400 mg or more per day) have been linked to increased risk of heart attack and stroke. The risk is increased with higher total daily doses and taking the medication over long periods of time. If you have had a heart attack or stroke, or are at risk of a heart attack or stroke, discuss with your doctor how Motrin Junior Strength (Ibuprofen) may affect your medical condition, how your medical condition may affect the dosing and effectiveness of Motrin Junior Strength (Ibuprofen), and whether any special monitoring is needed.

Heart disease: Motrin Junior Strength (Ibuprofen) can cause fluid retention, which may make symptoms of congestive heart failure worse. If you have been diagnosed with congestive heart failure, discuss with your doctor how Motrin Junior Strength (Ibuprofen) may affect your medical condition, how your medical condition may affect the dosing and effectiveness of Motrin Junior Strength (Ibuprofen), and whether any special monitoring is needed.

If you are taking low-dose ASA for heart health, discuss with your doctor whether you should use Motrin Junior Strength (Ibuprofen).

Kidney function: Long-term use of Motrin Junior Strength (Ibuprofen) may lead to a higher risk of reduced kidney function. This is most common for people who already have kidney disease, liver disease, or heart failure; for people who take diuretics (water pills); and for seniors.

If you have reduced kidney function or kidney disease, discuss with your doctor how Motrin Junior Strength (Ibuprofen) may affect your medical condition, how your medical condition may affect the dosing and effectiveness of Motrin Junior Strength (Ibuprofen), and whether any special monitoring is needed.

People with severely reduced kidney function and kidney disease should not take Motrin Junior Strength (Ibuprofen).

Potassium levels: There is a risk of high levels of potassium in the blood for people who take NSAIDs, including Motrin Junior Strength (Ibuprofen). People most at risk are seniors; those who have conditions such as Diabetes or kidney failure; and those taking beta-blockers (e.g., Metoprolol), angiotensin converting enzyme (ACE) inhibitors (e.g., Ramipril), or some diuretics (water pills). If you experience unexplained nausea, fatigue, muscle weakness or tingling sensations, contact your doctor as these are possible symptoms of too much potassium in the blood.

Reduced alertness/dizziness: Motrin Junior Strength (Ibuprofen) may cause drowsiness, dizziness or a sensation of spinning, any of which can affect your ability to drive or operate machinery. Avoid these and other hazardous tasks until you have determined how Motrin Junior Strength (Ibuprofen) affects you.

Pregnancy: Motrin Junior Strength (Ibuprofen) should not be used during pregnancy unless the benefits outweigh the risks. If you become pregnant while taking Motrin Junior Strength (Ibuprofen), contact your doctor immediately. Motrin Junior Strength (Ibuprofen), like other NSAIDs, must not be taken in the last 3 months of pregnancy.

Motrin Junior Strength (Ibuprofen) may reduce your ability to become pregnant. Taking Motrin Junior Strength (Ibuprofen) while trying to become pregnant is not recommended.

Breast-feeding: Motrin Junior Strength (Ibuprofen) may pass into breast milk in small quantities. If you are a breast-feeding mother and are taking Motrin Junior Strength (Ibuprofen), it may affect your baby. Talk to your doctor about whether you should continue breast-feeding.

Seniors: Seniors appear to have a higher risk of side effects with Motrin Junior Strength (Ibuprofen). The lowest effective dosage should be used under close medical supervision.