Label: REDICARE IBUPROFEN- ibuprofen 200mg tablet, film coated
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Contains inactivated NDC Code(s)
NDC Code(s): 71105-750-68 - Packager: Redicare LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated July 2, 2021
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Active Ingredient (in each tablet) Purpose
Ibuprofen 200 mg (NSAID) .........................................................................................pain reliever/fever reducer
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Uses
temporarily relieves minor aches and pains due to: ■ headache ■ muscular aches ■ backache ■ minor pain of arthritis ■ toothache ■ menstrual cramps ■ common cold ■ temporarily reduces fever
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Warnings
Allergy Alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: ■ hives ■ facial swelling ■ asthma (wheezing) ■ shock ■ skin ...
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Directions
Adults and children 12 years and older do not take more than directed - the smallest effective dose should be used - take 1 tablet every 4 to 6 hours while symptoms persist - If pain or fever does ...
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Other Information:
■ Tamper Evident. Do not use if packet is torn, cut or opened ■ Store at controlled room temperature 15˚ to 30˚C (59˚ to 86˚F) ■ Avoid excessive heat and humidity
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Inactive Ingredients:
Colloidal silicon dioxide, croscarmellose sodium, iron oxide red, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, pregelantinized starch, talc, titanium ...
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PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information