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ConRx Extra Strength

Dosage form: tablet
Ingredients: Acetaminophen 500mg
Labeler: Eagle Distributors,Inc.
NDC Code: 68737-233

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

ConRx™ Extra Strength

Important: Read all product information before using. Keep this box for important information.

Drug Facts

Active ingredient (in each caplet)

Acetaminophen 500 mg

Purpose

Pain reliever/fever reducer

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

Warnings

Liver warning

This product contains acetaminophen. The maximum daily dose of this product is 6 caplets (3,000 mg) in 24 hours. Severe liver damage may occur if you take

  • more than 4,000 mg of acetaminophen in 24 hours
  • 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 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 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.

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
  • do not take more than directed (see overdose warning)
    adults and children 12 years and over
    • take 2 caplets every 6 hours while symptoms last
    • do not take more than 6 caplets in 24 hours, unless directed by a doctor
    • do not use for more than 10 days unless directed by a doctor
  • children under 12 years, ask a doctor

Other information
  • store between 20-25˚C (68-77˚F)
  • do not use if pouch is torn or open
  • see side panel for lot number and expiration date

Inactive ingredients

carnauba wax*, castor oil*, corn starch, FD&C red #40 aluminum lake, hypromellose, magnesium stearate, polyethylene glycol*, powdered cellulose, pregelatinized starch, propylene glycol, shellac, sodium starch glycolate, titanium dioxide

  • contains one or more of these ingredients

Questions or comments?

1-800-570-8650

PRINCIPAL DISPLAY PANEL - 50 Pouch Box

See New Warnings Information & Directions

Compate to the Active Ingredients in
Tylenol® Extra Strength *

ConRx™

EXTRA
STRENGTH

DO NOT USE WITH OTHER MEDICINES CONTAINING ACETAMINOPHEN
Acetaminophen
Pain Reliever - Fever Reducer

CONRX EXTRA STRENGTH 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68737-233
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (Acetaminophen) Acetaminophen500 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX 
CASTOR OIL 
STARCH, CORN 
FD&C Red NO. 40 
ALUMINUM OXIDE 
HYPROMELLOSES 
MAGNESIUM STEARATE 
POLYETHYLENE GLYCOL 6000 
POWDERED CELLULOSE 
PROPYLENE GLYCOL 
SHELLAC 
SODIUM STARCH GLYCOLATE TYPE A CORN 
TITANIUM DIOXIDE 
Product Characteristics
ColorREDScore2 pieces
ShapeOVALSize18mm
FlavorImprint CodeCRX
Contains    
Packaging
#Item CodePackage Description
1NDC:68737-233-1750 POUCH in 1 BOX
12 TABLET in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34302/15/2013
Labeler - Eagle Distributors,Inc. (929837425)

 
Eagle Distributors,Inc.

Medically reviewed on Feb 12, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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