Label: ARTHRITIS PAIN- acetaminophen tablet, extended release
- NDC Code(s): 21130-124-02, 21130-124-03
- Packager: SAFEWAY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated October 30, 2023
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SPL UNCLASSIFIED SECTIONDrug Facts
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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 - muscular aches - backache - premenstrual and menstrual cramps - the common ...
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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 ...
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Other informationstore between 20-25°C (68-77°F) retain carton for complete product information and warnings
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Inactive ingredientshydroxyethyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, pregelatinized starch, sodium starch glycolate, stearic acid
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Questions or comments?1-844-705-4384
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PRINCIPAL DISPLAY PANELsignature care® Quality Guaranteed - NDC 21130-124-02 - 8 Hour - Arthritis Pain - Compare to the active ingredient in Tylenol® 8HR Arthritis Pain* ACETAMINOPHEN - Extended-Release Tablets, 650mg - Pain ...
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INGREDIENTS AND APPEARANCEProduct Information