Label: IBUPROFEN 200 MG- ibuprofen tablet, coated
- NDC Code(s): 70264-042-01
- Packager: R J General Corporation
- This is a repackaged label.
- Source NDC Code(s): 0573-0150
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2024
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- Official Label (Printer Friendly)
- Drug facts
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ACTIVE INGREDIENTActive ingredients (in each tablet)Purpose - * nonsteroidal anti-inflammatory drug - Ibuprofen 200 mg (NSAID) *Pain reliever/Fever reducer
- PURPOSE
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Uses
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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Warnings
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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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
read all warnings and directions before use. Keep Carton. store at 20-25°C (68-77°F) avoid excessive heat above 40°C (104°F)
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Inactive ingredients
acetylated monoglycerides, colloidal silicon dioxide, corn starch, croscarmellose sodium, methylparaben, microcrystalline cellulose, pharmaceutical glaze, pharmaceutical ink, povidone ...
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Questions or Comments?
Call toll free - 1-800-88-ADVIL - Distributed by: GSK CH, Warren, NJ 07059 - Packaged and distributed by RJ Corp with the permission of HALEON.
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PRINCIPAL DISPLAY PANELIbuprofen 200 mg - NDC 70264-042-01 - Carton Label
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INGREDIENTS AND APPEARANCEProduct Information