Label: IBUPROFEN tablet, film coated
- NDC Code(s): 50844-257-15
- Packager: L.N.K. International, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated April 16, 2025
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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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Purpose
Pain reliever/fever reducer
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Uses
temporarily relieves minor aches and pains due to: menstrual cramps - toothache - the common cold - backache - headache - muscular aches - minor pain of arthritis - 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: shock - skin reddening - asthma (wheezing) rash - facial ...
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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 does ...
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Other information
store between 20°-25°C (68°-77°F) avoid excessive heat 40°C (104°F) see end flap for expiration date and lot number
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Inactive ingredients
carnauba wax, colloidal silicon dioxide, corn starch, hypromellose, lactose anhydrous, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, red iron oxide, sodium ...
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Questions or comments?
1-844-428-2538
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Principal Display Panel
24/7 life - BY 7-ELEVEN™ Ibuprofen - Ibuprofen Tablets USP, 200 mg - Pain Reliever/Fever Reducer (NSAID) compare to - ADVIL® TABLETS - active ingredient** 50 - TABLETS - Actual ...
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INGREDIENTS AND APPEARANCEProduct Information