Label: IBUPROFEN tablet, film coated
- NDC Code(s): 68210-4201-2
- Packager: Spirit Pharmaceuticals LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated December 13, 2024
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- Official Label (Printer Friendly)
- Drug Facts
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Active Ingredient (in each tablet)
Ibuprofen 200 mg (NSAID)** **nonsteroidal anti-inflammatory drug
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Purpose
Pain reliever/fever reducer
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Uses
• temporarily relieves minor aches and pains due to: • headache • toothache • backache - • menstrual cramps • the common cold • muscular aches • minor pain of arthritis • temporarily ...
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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 ...
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Directions
• do not take more than directed • the smallest effective dose should be used • adults and children 12 years and over: take 1 tablet every 4 to 6 hours while symptoms persist • if pain or fever ...
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Other Information
• read all warnings and directions before use. Keep carton. • store between 20°-25°C (68°-77°F) • avoid excessive heat above 40°C (104°F)
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Inactive ingredients
Colloidal silicon dioxide, corn starch, hypromellose, red iron oxide, magnesium stearate*, microcrystalline cellulose*, povidone K-30*, pregelatinized starch, sodium starch glycolate ...
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Questions or comments?
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Principal Display Label - Carton
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INGREDIENTS AND APPEARANCEProduct Information