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Acetaminophen - Medication Information

Product NDC Code 11673-342
Drug Name

Acetaminophen

Type Generic
Active Ingredients
Acetaminophen 500 mg/1
Route ORAL
Dosage Form TABLET, FILM COATED
RxCUI drug identifier 198440
Application Number part343
Labeler Name TARGET CORPORATION
Packages
Package NDC Code Description
11673-342-01 100 tablet, film coated in 1 bottle (11673-342-01)
11673-342-26 225 tablet, film coated in 1 bottle (11673-342-26)
11673-342-42 24 tablet, film coated in 1 bottle (11673-342-42)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENTS Active Ingredient: Each tablet contains Acetaminophen 500 mg
Active Ingredient: Each tablet contains Acetaminophen 500 mg

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Do not take more than directed (see overdosage warning) Adults and children 12 years and over: take 2 tablets (1,000 mg) every 6 hours while symptoms last; do not take more than 6 tablets (3,000 mg) in 24 hours, unless directed by a doctor; do not take for more than 10 days unless directed by a doctor Children under 12 years: Do not use this adult extra strength product in children under 12 years of age, this will provide more than the recommended dose (overdosage) of acetaminophen and may cause liver damage
Do not take more than directed (see overdosage warning) Adults and children 12 years and over: take 2 tablets (1,000 mg) every 6 hours while symptoms last; do not take more than 6 tablets (3,000 mg) in 24 hours, unless directed by a doctor; do not take for more than 10 days unless directed by a doctor Children under 12 years: Do not use this adult extra strength product in children under 12 years of age, this will provide more than the recommended dose (overdosage) of acetaminophen and may cause liver damage

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENTS CARNAUBA WAX, FD-C RED NO. 40 ALUMINUM LAKE, HYPROMELLOSE, POLYETHYLENE GLYCOL(PEG) 400, POLYETHYLENE GLYCOL (peg) 8000, POVIDONE, PREGELATINIZED STARCH, SODIUM STARCH GLYCOLATE**, STEARIC ACID, SUCRALOSE, TITANIUM DIOXIDE ** MAY CONTAIN THIS INGREDIENT

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
INDICATIONS AND USAGE: Pain Reliever – temporarily relieves minor aches and pains due to: the common cold, headache, backache, muscular aches, toothache, premenstrual and menstrual cramps, minor pain of arthritis. Temporarily reduces fever.
INDICATIONS AND USAGE: Pain Reliever – temporarily relieves minor aches and pains due to: the common cold, headache, backache, muscular aches, toothache, premenstrual and menstrual cramps, minor pain of arthritis. Temporarily reduces fever.

Purpose

Information about the drug product’s indications for use.
PURPOSE: Pain Reliever - fever reducer
PURPOSE: Pain Reliever - fever reducer

Spl product data elements

Usually a list of ingredients in a drug product.
ACETAMINOPHEN ACETAMINOPHEN POLYETHYLENE GLYCOL 8000 ACETAMINOPHEN ACETAMINOPHEN HYPROMELLOSES POLYETHYLENE GLYCOL 400 STARCH, CORN SODIUM STARCH GLYCOLATE TYPE A POTATO STEARIC ACID SUCRALOSE TITANIUM DIOXIDE CARNAUBA WAX FD&C RED NO. 40 POVIDONE TCL342

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
24 CT 225 CT 100CT

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep Out of the Reach of Children: In case of overdose, get medical help or contact a Poison Control Center right away
Keep Out of the Reach of Children: In case of overdose, get medical help or contact a Poison Control Center right away

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings; Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take: more than 8 tablets in 24 hours, which is the maximum daily amount; 3 or more alcoholic drinks every day while using this product; with other drugs containing acetaminophen. Overdose warning: Taking more than the recommended dose (0verdose) may cause liver damage. in case of overdose, get medical help or contact a Poison Control Center (1-800-222-1221) right way. Quick medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.
Warnings; Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take: more than 8 tablets in 24 hours, which is the maximum daily amount; 3 or more alcoholic drinks every day while using this product; with other drugs containing acetaminophen. Overdose warning: Taking more than the recommended dose (0verdose) may cause liver damage. in case of overdose, get medical help or contact a Poison Control Center (1-800-222-1221) right way. Quick medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API