Label: IBUPROFEN tablet, coated
- NDC Code(s): 72476-109-01, 72476-109-02, 72476-109-03, 72476-109-05, view more
- Packager: RETAIL BUSINESS SERVICES , LLC.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 5, 2021
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- Official Label (Printer Friendly)
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SPL UNCLASSIFIED SECTIONDrug Facts
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Active ingredient (in each tablet)Ibuprofen 200 mg (NSAID)* * nonsteroidal anti-inflammatory drug
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PurposePain reliever/fever reducer
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Usestemporarily relieves minor aches and pains due to: headache - toothache - backache - menstrual cramps - the common cold - muscular aches - minor pain of ...
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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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Directions■ do not take more than directed - ■ the smallest effective dose should be used - ■ adults and children 12 years and over: ■ take 1 tablet ...
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Other informationstore at 20°-25°C (68°-77°F) avoid excessive heat above 40°C (104°F) read all warnings and directions before use - retain carton for complete product information and warnings
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Inactive ingredientscolloidal silicon dioxide, corn starch, iron oxide red, polyethylene glycol, polyvinyl alcohol, povidone K30, pregelatinized starch, sodium starch glycolate, stearic acid, talc, titanium ...
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PRINCIPAL DISPLAY PANEL(What is this?)CAREONE® NDC 72476-109-01 - Compare to the active ingredient in Advil® Ibuprofen Tablets† IBUPROFEN - Tablets, 200 mg - Pain Reliever / Fever Reducer - (NSAID) Actual Size - 24 TABLETS
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INGREDIENTS AND APPEARANCEProduct Information