Label: PAIN RELIEF EXTRA STRENGTH- acetaminophen tablet, coated
- NDC Code(s): 83324-079-50
- Packager: CHAIN DRUG MARKETING ASSOCIATION, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 13, 2024
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SPL UNCLASSIFIED SECTIONDrug Facts
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Active ingredient (in each caplet)Acetaminophen 500 mg
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PurposePain reliever/fever reducer
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Usestemporarily relieves minor aches and pains due to: the common cold - headache - backache - minor pain of arthritis - toothache - muscular aches - premenstrual and menstrual cramps - temporarily ...
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WarningsLiver warning - This product contains acetaminophen. Severe liver damage may occur if you take - more than 4,000 mg of acetaminophen in 24 hours - with other drugs containing acetaminophen - 3 or more ...
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Directionsdo not take more than directed (see - overdose warning) adults and children 12 years and over - take 2 caplets every 6 hours while symptoms last - swallow whole – do not crush ...
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Other informationstore between 20-25°C (68-77°F) retain carton for complete product information
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Inactive ingredientsacesulfame potassium, flavor, hypromellose, polyethylene glycol, povidone, pregelatinized starch, propylene glycol, sodium starch glycolate, stearic acid, titanium dioxide
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PRINCIPAL DISPLAY PANELQUALITY CHOICE® NDC 83324-079-50 - †Compare to Active Ingredient in TYLENOL® Extra Strength - For Adults - Extra Strength - Pain Relief - Acetaminophen - Pain Reliever | Fever Reducer - Instant Cooling ...
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INGREDIENTS AND APPEARANCEProduct Information