DrugCite

ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE - acetaminophen and phenylephrine hydrochloride tablet, coated 
AAA Pharmaceutical, Inc.

Acetaminophen, Phenylephrine HCl Tablets

Drug Facts

Active ingredients (in each caplet) Purpose
Acetaminophen 325 mg Pain reliever
Phenylephrine HCl 5 mg Nasal decongestant

Uses

  • temporarily relieves
    • sinus congestion and pressure
    • headache
    • minor aches and pains
    • nasal congestion

Warnings

Liver warning

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

  • more than 12 caplets 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

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 now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

  • liver disease
  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes
  • trouble urinating due to an enlarged prostate gland

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin

When using this product do not exceed the recommended dosage

Stop use and ask a doctor if

  • nervousness, dizziness, or sleeplessness occur
  • pain or nasal congestion gets worse or lasts more than 7 days
  • redness or swelling is present
  • fever gets worse or lasts more than 3 days
  • new symptoms occur

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.

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 for children even if you do not notice any signs or symptoms.

Directions

adults and children 12 years and over
  • take 2 caplets every 4 hours
  • do not take more than 12 caplets in 24 hours
children under 12 years
  • do not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage

Other information

  • store between 20°-25°C (68°-77°F) in a dry place
  • retain carton for complete product information

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, FD&C yellow #6, hypromellose, lactose anhydrous, magnesium stearate, methylparaben, povidone, pregelatinized starch, propylene glycol, propylparaben, sodium starch glycolate, stearic acid, titanium dioxide, triacetin

Distributed by:
AAA Pharmaceutical, Inc.
681 Main Street
Lumberton, NJ 08048

PRINCIPAL DISPLAY PANEL - 24 Caplet Blister Pack Carton

RESTORE u

NDC 57344-154-02

COMPARE TO THE ACTIVE
ACTIVE INGREDIENTS
IN SINUTAB® SINUS

NON-DROWSY

Maximum Strength
Sinus Relief

Pain Reliever, Nasal Decongestant
Acetaminophen, Phenylephrine HCI

Relieves: • Headache • Nasal Congestion
• Sinus Presssure & Pain

24 CAPLETS

Principal Display Panel - 24 Caplet Blister Pack Carton

ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE 
acetaminophen and phenylephrine hydrochloride  tablet, coated
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 57344-154
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN 325 mg
PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE) PHENYLEPHRINE HYDROCHLORIDE 5 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE  
CROSCARMELLOSE SODIUM  
FD&C YELLOW NO. 6  
HYPROMELLOSES  
ANHYDROUS LACTOSE  
MAGNESIUM STEARATE  
METHYLPARABEN  
POVIDONES  
STARCH, CORN  
PROPYLENE GLYCOL  
PROPYLPARABEN  
SODIUM STARCH GLYCOLATE TYPE A CORN  
STEARIC ACID  
TITANIUM DIOXIDE  
TRIACETIN  
Product Characteristics
Color ORANGE Score no score
Shape OVAL Size 17mm
Flavor Imprint Code AAA;1114
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 57344-154-02 2  In 1 CARTON contains a BLISTER PACK
1 12  In 1 BLISTER PACK This package is contained within the CARTON (57344-154-02)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part341 12/22/2012

Labeler - AAA Pharmaceutical, Inc. (181192162)
Establishment
Name Address ID/FEI Operations
AAA Pharmaceutical, Inc. 181192162 MANUFACTURE
Establishment
Name Address ID/FEI Operations
AAA Pharmaceutical, Inc. 010411533 PACK
Revised: 01/2013AAA Pharmaceutical, Inc.