Amazon Basic Care Acetaminophen

Acetaminophen · Tablet · Oral

Over the counter 1 recall

Active ingredient

Drug Facts Active ingredient (in each extended-release tablet) Acetaminophen USP 650 mg

Purpose

Purpose Pain reliever/fever reducer

Uses

Uses temporarily relieves minor aches and pains due to: muscular aches backache minor pain of arthritis toothache premenstrual and menstrual cramps headache the common cold temporarily reduces fever

Warnings

Warnings Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take more than 6 tablets in 24 hours, which is the maximum daily amount with other drugs containing acetaminophen 3 or more alcoholic drinks every day while using this product Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include: skin reddening blisters rash If a skin reaction occurs, stop use and seek medical help right away.

Do not use

Do not use with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. if you are allergic to acetaminophen or any of the inactive ingredients in this product. Ask a doctor before use if you have liver disease. Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin

Stop use and ask a doctor

Stop use and ask a doctor if pain gets worse or lasts more than 10 days fever gets worse or lasts more than 3 days new symptoms occur redness or swelling is present These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children

Keep out of reach of children. Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222) Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

Directions do not take more than directed (see overdose warning). adults and children 12 years and over take 2 tablets every 8 hours with water swallow whole; do not crush, chew, split or dissolve do not take more than 6 tablets in 24 hours do not use for more than 10 days unless directed by a doctor. children under 12 years do not use

Other information

Other information store at 20 o to 25 o C (68 o to 77 o F). Avoid excessive heat 40 o C (104 o F). do not use if carton is opened or foil inner seal is broken Meets USP dissolution test 3

Inactive ingredients

Inactive ingredients colloidal silicon dioxide, hydroxyethyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch (maize), sodium starch glycolate, titanium dioxide, triacetin Questions or comments? call 1-855-274-4122 DISTRIBUTED BY: AMAZON.COM SERVICES LLC 410 TERRY AVENUE N., SEATTLE, WA 98109 ©2024 AMAZON.COM, INC. OR ITS AFFILIATES. ALL RIGHTS RESERVED. Made in India

Label text from the FDA structured product label by Amazon.com Services LLC (revised May 14, 2024). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Amazon Basic Care Acetaminophen NDC products (3)

NDCStrength & formLabelerType
72288-698Acetaminophen 650 mg/1
Tablet, Extended Release
Amazon.com Services LLCANDA
72288-405Acetaminophen 325 mg/1
Tablet
Amazon.com Services LLCOTC MONOGRAPH DRUG
72288-692Acetaminophen 500 mg/1
Tablet
Amazon.com Services LLCOTC MONOGRAPH DRUG

Amazon Basic Care Acetaminophen recalls

Frequently asked questions

What is Amazon Basic Care Acetaminophen used for?

Uses temporarily relieves minor aches and pains due to: muscular aches backache minor pain of arthritis toothache premenstrual and menstrual cramps headache the common cold temporarily reduces fever

Who makes Amazon Basic Care Acetaminophen?

Amazon Basic Care Acetaminophen is listed by 1 labeler in the FDA NDC directory, including Amazon.com Services LLC.

Has Amazon Basic Care Acetaminophen been recalled?

The FDA enforcement database lists 1 recall for Amazon Basic Care Acetaminophen, most recently D-0471-2025 (class ii): cGMP deviations: Due to confirmed consumer complaints received with the observation of tablet discoloration (brown surface on tablets).