Label: IBUPROFEN 200MG tablet
- NDC Code(s): 69168-467-03, 69168-467-05, 69168-467-32
- Packager: Allegiant Health
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated September 30, 2024
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- Official Label (Printer Friendly)
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Active ingredient(s)Ibuprofen USP, 200mg (NSAID)* *nonsteroidal anti-inflammatory drug
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PurposePain Reliever/Fever reducer
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Use(s)temporarily 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: hives - facial swelling - asthma (wheezing) shock - skin ...
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Directionsdo 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 does not ...
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Other informationstore between 20-25 °C (68-77° F) read all warnings and directions before use - do not use if seal under bottle cap is broken or missing
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Inactive ingredientsColloidal Silicon Dioxide, Croscarmellose Sodium, FD&C - Blue #2, FD&C Yellow #5, FD&C Yellow #6, Iron Oxide Red, Lecithin, Magnesium - Stearate, Microcrystalline Cellulose, Polyethylene Glycol ...
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Questions/CommentsCall 1-888-952-0050 Monday through Friday 9AM – 5PM EST
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Principal Display PanelIbuprofen
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INGREDIENTS AND APPEARANCEProduct Information