Label: ARTHRITISPAIN RELIEF- acetaminophen tablet
- NDC Code(s): 59726-669-10
- Packager: P & L Development, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 1, 2024
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- Official Label (Printer Friendly)
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Active ingredient (in each caplet)Acetaminophen 650 mg
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PurposePain reliever/fever reducer
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Usestemporarily relieves minor aches and pains due to: minor pain of arthritis - backache - muscular aches - toothache - premenstrual and menstrual cramps - headache - the common cold - temporarily reduces ...
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WarningsLiver warning: This product contains acetaminophen. Severe liver damage may occur if you take: more than 6 caplets in 24 hours, which is the maximum daily amount - with other drugs containing ...
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Directionsdo not take more than directed (see Overdose warning) adults - take 2 caplets every 8 hours with water - swallow whole; do not crush, chew, split or dissolve - do not take more than 6 caplets in ...
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Other informationstore between 20-25°C (68-77°F)
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Inactive ingredientsD&C yellow #10 aluminum lake, FD&C yellow #6 aluminum lake, hydroxyethyl cellulose, magnesium stearate, maize starch, microcrystalline cellulose, povidone, pregelatinized starch, sodium lauryl ...
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Questions or comments?Call 1-877-753-3935 Monday-Friday 9AM-5PM EST
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Principal Display PanelCompare to the active ingredient of Tylenol® 8HR Arthritis Pain† extended-release - arthritis pain reliever - acetaminophen 650 mg - pain reliever/fever reducer - for the temporary relief of ...
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Product LabelREADYinCASE Arthritis Pain Reliever
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INGREDIENTS AND APPEARANCEProduct Information