Label: IBUPROFEN capsule, liquid filled
- NDC Code(s): 41226-700-80, 41226-700-87
- Packager: KROGER COMPANY
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated April 13, 2024
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- Official Label (Printer Friendly)
- Drug Facts
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ACTIVE INGREDIENTActive ingredient (in each capsule) Solubilized ibuprofen equal to - 200 mg ibuprofen (NSAID)* (present as the free acid and potassium salt) *nonsteroidal anti-inflammatory drug
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PURPOSEPurpose - Pain reliever/Fever reducer
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INDICATIONS & USAGEUses - 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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WARNINGSWarnings - Allergy 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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DOSAGE & ADMINISTRATIONDirections - do not take more than directed - the smallest effective dose should be used - adults and children 12 years and over: take 1 capsule every 4 to 6 hours while symptoms persist - if pain ...
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STORAGE AND HANDLINGOther information - each capsule contains:potassium 20 mg - read all warnings and directions before use - store at 20-25ºC (68-77ºF) avoid excessive heat above 40°C (104°F).
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INACTIVE INGREDIENTInactive ingredientsammonium hydroxide, FD&C green no.3, gelatin, iron oxide black, medium chain triglycerides, polyethylene glycol, potassium hydroxide, propylene glycol, purified water, shellac ...
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QUESTIONSQuestions or comments? Call - 1-800-632-6900
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INGREDIENTS AND APPEARANCEProduct Information