Label: IBUPROFEN tablet, film coated
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Contains inactivated NDC Code(s)
NDC Code(s): 76413-345-01 - Packager: Central Texas Community Health Centers
- This is a repackaged label.
- Source NDC Code(s): 57896-941
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated September 12, 2017
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- Official Label (Printer Friendly)
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Active ingredient (in each brown tablet)Ibuprofen USP, 200 mg (NSAID)* *nonsteroidal anti-inflammatory drug
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PurposePain reliever/fever reducer
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UsesTemporarily relieves minor aches and pains due to: headache - toothache - backache - menstrual cramps - the common cold - muscular aches - minor pain of arthritis - Temporarily reduces fever
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WarningsAllergy Alert: Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: shock - hives - facial swelling - asthma (wheezing) skin ...
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Directionsdo not use more than directed - the smallest effective dose should be used - do not take longer than 10 days, unless directed by a doctor (see Warnings) adults and children 12 years and over ...
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Other informationstore at controlled room temperature - avoid excessive heat 40°C (104°F)
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Inactive ingredientscarnauba wax, cellulose, corn starch, fumed silica gel, hypromellose, lactose, magnesium stearate, polydextrose, PEG, red iron oxide, sodium starch glycolate, stearic acid, titanium ...
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PRINCIPAL DISPLAY PANEL - 200 MG Tablet Bottle Box Label(What is this?)CommUnityCare Federally Qualified Health Centers - IBUPROFEN - 200MG - TABS #100 - Date: Name: Dr. TAKE AS DIRECTED. 1/1/01 - 123456 - IBUPROFEN 200MG TABS #100 NDC ...
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INGREDIENTS AND APPEARANCEProduct Information