Label: ACETAMINOPHEN EXTRA STRENGTH- acetaminophen tablet, film coated
- NDC Code(s): 69842-931-08, 69842-931-17, 69842-931-29
- Packager: CVS PHARMACY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 18, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
Active ingredient (in each tablet)
Acetaminophen 500 mg
-
Purpose
Pain reliever/fever reducer
-
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 ...
-
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 ...
-
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 doctor - do ...
-
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
-
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 ...
-
Questions or comments?
1-800-426-9391
-
Principal display panel
CVS™ 69842-931-08 - Extra Strength - ACETAMINOPHEN - Pain Reliever, Fever Reducer, 500 mg - 24 FILM - COATED TABLETS - Contains No Aspirin - TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY - SEAL UNDER ...
-
INGREDIENTS AND APPEARANCEProduct Information