Label: PAIN RELIEF- acetaminophen tablet, film coated
- NDC Code(s): 55910-135-15
- Packager: DOLGENCORP, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 7, 2024
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- Official Label (Printer Friendly)
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Active ingredient (in each tablet)
Acetaminophen 500 mg
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Purpose
Pain reliever/fever reducer
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Uses
temporarily relieves minor aches and pains due to - headache - toothache - muscular aches - backache - the common cold - minor pain of arthritis - premenstrual and menstrual cramps - temporarily reduces ...
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Warnings
Liver 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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Directions
do not take more than directed - adults and children 12 years and over - take 2 tablets every 6 hours while symptoms last - do not take more than 6 tablets in 24 hours, unless directed by a ...
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Other information
store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F) see end flap for expiration date and lot number
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Inactive ingredients
corn starch, D&C red #27 aluminum lake, D&C yellow #10 aluminum lake, FD&C blue #1 aluminum lake, polyethylene glycol, polyvinyl alcohol, povidone, sodium starch glycolate*, stearic acid ...
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Questions or comments?
1-888-309-9030
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Principal display panel
DG® | health - Compare to - active ingredient of - Extra Strength - Tylenol®** Extra Strength - Pain Relief - Acetaminophen, 500 mg - Pain Reliever/Fever Reducer - • Contains no aspirin - 500 - mg ...
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INGREDIENTS AND APPEARANCEProduct Information