Label: IBUPROFEN tablet, film coated
- NDC Code(s): 55319-893-12
- Packager: Family Dollar Services Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 13, 2024
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- Official Label (Printer Friendly)
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Active ingredient (in each orange caplet)
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: headache - backache - menstrual cramps - toothache - the common cold - 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: facial swelling - blisters - hives - shock - skin reddening - 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 caplet 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, FD&C yellow #6 aluminum lake, hypromellose, lactose anhydrous, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene ...
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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
Family - Wellness™ †COMPARE TO THE - ACTIVE INGREDIENT IN - MOTRIN® IB CAPLETS - IBUPROFEN - Ibuprofen Tablets USP, 200 mg - Pain Reliever/Fever Reducer (NSAID) ACTUAL SIZE - Film Coated ...
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INGREDIENTS AND APPEARANCEProduct Information