FDA Label for Acetaminophen

View Indications, Usage & Precautions

Acetaminophen Product Label

The following document was submitted to the FDA by the labeler of this product Pai Holdings, Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Other



Drug Facts


Active Ingredient (In Each 5 Ml Teaspoonful)



Acetaminophen 160 mg


Purpose



Pain reliever/fever reducer


Uses



temporarily relieves minor aches and pains due to:

  • headache
  • muscular aches
  • backache
  • minor pain of arthritis
  • the common cold
  • toothache
  • premenstrual and menstrual cramps
  • temporarily reduces fever


Liver Warning



This product contains acetaminophen. Severe liver damage may occur if you take:

  • adult takes more than 6 doses in 24 hours, which is the maximum daily amount
  • child takes more than 5 doses in 24 hours
  • 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.


Sore Throat Warning



If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.


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.
  • for more than 10 days for pain unless directed by a doctor
  • for more than 3 days for fever unless directed by a doctor
  • if you are allergic to acetaminophen or any of the inactive ingredients of 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 If



  • symptoms do not improve
  • new symptoms occur
  • pain or fever persists or gets worse

Otc - Pregnancy Or Breast Feeding



If pregnant or breast-feeding, ask a health professional before use.


Otc - Keep Out Of Reach Of Children



Keep out of reach of children.


Overdose Warning



Taking more than the recommended dose (overdose) may cause liver damage. 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 children even if you do not notice any signs or symptoms.


Directions



  • do not take more than directed (see overdose warning)
  • agedose
    adults and children 12 years of age and over20.3 mL (650 mg) every 4 to 6 hours
    not to exceed 6 doses in a 24-hour period
    children 6 to under 12 years of age10.15 mL (325 mg) every 4 hours
    not to exceed 5 doses in a 24-hour period
    children 4 to under 6 years of age7.5 mL (240 mg) every 4 hours
    not to exceed 5 doses in a 24-hour period
    children 2 to under 4 years of age5 mL (160 mg) every 4 hours
    not to exceed 5 doses in a 24-hour period
    children under 2 years of ageconsult a doctor


Other Information



sodium content: 2 mg/5 mL 

■ store at 20° to 25°C (68° to 77°F). [See USP controlled room temperature]

■ keep tightly closed  ■ protect from light

■ a red, cherry flavored solution supplied in the following oral dosage forms:

NDC 0121-0657-05:  5 mL unit dose cup

NDC 0121-0657-00:   Case contains 100 unit dose cups of 5 mL (0121-0657-05) packaged in 10 trays of 10 unit dose cups each.

NDC 0121-1314-11:  10.15 mL unit dose cup

NDC 0121-1314-00:   Case contains 100 unit dose cups of 10.15 mL (0121-1314-11) packaged in 10 trays of 10 unit dose cups each.

NDC 0121-1971-21:  20.3 mL unit dose cup

NDC 0121-1971-00:   Case contains 100 unit dose cups of 20.3 mL (0121-1971-21) packaged in 10 trays of 10 unit dose cups each.


Inactive Ingredients



Citric acid, FD&C Red No. 40, flavoring, glycerin, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol and sucrose.


Questions Or Comments?



Call 1-800-845-8210. You may also report serious side effects to this phone number.


Manufactured By:



Pharmaceutical Associates, Inc.

Greenville, SC 29605

www.paipharma.com

R01/17


Principal Display Panel - 20 Ml Cup



Delivers 20.3 mL

NDC 0121-1971-21

A CETAMINOPHEN

O RAL S OLUTION USP

650 mg/20.3 mL

ALCOHOL FREE

FOR INSTITUTIONAL USE ONLY

PHARMACEUTICAL ASSOCIATES, INC.
GREENVILLE, SC 29605

SEE INSERT

F06572102


Principal Display Panel - 10 Ml Cup



Delivers 10.15 mL

NDC 0121-1314-11

A CETAMINOPHEN

O RAL S OLUTION USP

325 mg/10.15 mL

ALCOHOL FREE

FOR INSTITUTIONAL USE ONLY

PHARMACEUTICAL ASSOCIATES, INC.
GREENVILLE, SC 29605

SEE INSERT

F06571102


Principal Display Panel - 5 Ml Cup



Delivers 5 mL

NDC 0121-0657-05

A CETAMINOPHEN

O RAL S OLUTION USP

160 mg/5 mL

ALCOHOL FREE

FOR INSTITUTIONAL USE ONLY

PHARMACEUTICAL ASSOCIATES, INC.
GREENVILLE, SC 29605

SEE INSERT

A06570500


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