Label: IBUPROFEN tablet, film coated
- NDC Code(s): 11822-0291-0, 11822-0291-1, 11822-0291-2, 11822-0291-3, view more
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated June 2, 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: muscular aches - headache - menstrual cramps - backache - the common cold - toothache - 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: facial swelling - shock - hives - asthma (wheezing) skin ...
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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
see end flap for expiration date and lot number - store between 20°-25°C (68°-77°F) avoid excessive heat 40°C (104°F)
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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?
Call 1-800-426-9391 8:30 AM-4:00 PM ET, Monday-Friday
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Principal Display Panel
TRIAL SIZE - NDC 11822-0291-2 - Compare to the - active ingredient in - Advil® Tablets** PAIN RELIEF - IBUPROFEN - IBUPROFEN TABLETS USP, 200 mg - PAIN RELIEVER/FEVER REDUCER - (NSAID) ACTUAL ...
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INGREDIENTS AND APPEARANCEProduct Information