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Acetaminophen - Medication Information

Product NDC Code 17714-012
Drug Name

Acetaminophen

Type Generic
Active Ingredients
Acetaminophen 325 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 313782
Application Number part343
Labeler Name Advance Pharmaceutical Inc.
Packages
Package NDC Code Description
17714-012-01 100 tablet in 1 bottle (17714-012-01)
17714-012-10 1000 tablet in 1 bottle (17714-012-10)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient (in each tablet) Acetaminophen 325 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.
Directions adults and children 12 years and over 1-2 tablets every 4 hours or 2-3 tablets every 6 hours while symptoms last, not more than 12 tablets in 24 hours children 6 to 11 years 1 tablet every 4 hours while symptoms last, not more than 5 tablets in 24 hours children under 6 years ask a doctor
adults and children 12 years and over 1-2 tablets every 4 hours or 2-3 tablets every 6 hours while symptoms last, not more than 12 tablets in 24 hours
children 6 to 11 years 1 tablet every 4 hours while symptoms last, not more than 5 tablets in 24 hours
children under 6 years ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients polyvinylpyrrolidone, pregelatinized corn starch, sodium starch glycolate, stearic acid

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.
Uses temporarily reduces fever and relieves minor aches and pains caused by common cold headache toothache muscular aches premenstrual and menstrual cramps

Purpose

Information about the drug product’s indications for use.
Purpose Pain Reliever / Fever Reducer

Spl product data elements

Usually a list of ingredients in a drug product.
Acetaminophen Acetaminophen POVIDONE STARCH, CORN SODIUM STARCH GLYCOLATE TYPE A POTATO STEARIC ACID ACETAMINOPHEN ACETAMINOPHEN AP;012

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.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC: 17714-012-01 – 100 COUNT NDC: 17714-012-10 – 1000 COUNT 1d2e4055-figure-01 1d2e4055-figure-02 1d2e4055-figure-03

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Other Information store at 15-30 °C (59-86 °F) For Bulk package: This is a bulk package, dispense contents with a child-resistant closure in a tight, light resistant container as defined in the USP.

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 reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children, even if you do not notice any signs or symptoms.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or Comments TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING Manufactured by: Advance Pharmaceutical, Inc. Holtsville, NY 11742

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 adult takes more than 12 tablets in 24 hours, which is the maximum daily amount child takes more than 5 tablets in 24 hours, which is the maximum daily amount taken with other drugs containing acetaminophen adult has 3 or more alcoholic drinks every day while using this product do not use with any other drug containing acetaminophen (prescription or non prescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. Ask a doctor before use if the user has liver disease Ask a doctor or pharmacist before use if the user is taking the blood thinning drug warfarin Stop use and ask a doctor if adult’s pain gets worse or lasts more than 10 days child’s pain gets worse or lasts more than 5 days fever gets worse or lasts more than 3 days redness or swelling is present any new symptoms appear If pregnant or breast-feeding, ask a health professional before use.

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