CONRX  ALLERGY SINUS MULTI-SYMPTOMS- acetaminophen, chlorpheniramine maleate, and phenylephrine hydrochloride tablet 
Eagle Distributors,Inc.

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.

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ConRx Allergy Sinus Multi-Symptoms

Drug Facts

Active ingredient (in each tablet)

Acetaminophen 325mg

Chlorpheniramine maleate 2mg

Phenylephrine HCl 5mg

Purpose

Pain reliever/ fever reducer

Antihistamine

Nasal decongestant

Uses

Uses For the temporary relieves these symptoms of hay fever or other upper respiratory allergies, headache, sinus congestion and pressure, nasal congestion, runny nose and sneezing ,minor aches and pains, itching of the nose or throat ,itchy watery eyes, help decongest sinus openings and passages.

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 for this product
  • 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.
  • If you have ever had an allergic reaction to this product or any of its ingredients

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
  • a breathing problem such as emphysema or chronic bronchitis,
  • glaucoma

Ask a doctor or pharmacist before use if you are taking

  • the blood thinning drug warfarin

When using this product

  • do not exceed recommended dosage
  • excitability may occur, especially in children
  • drowsiness may occur
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • avoid alcoholic drinks
  • be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if

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

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

Keep out of reach of children.

Overdose warning

In case of overdose, get medical help or contact a Poison 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.

Directions

Do not taking more than directed (see overdose warning)

Adults and Children 12 years and above
  • Take 1-2 tablets every 4 hours
  • Do not taking more than 8 tablets in 24 hour
Children under 12 years of ageConsult a doctor

Other Information

Inactive ingredients

Colloidal silicon dioxide, Sodium Lauryl Sulphate, Edetaet disodium, Dioctyl Sodium Sulphosuccinate, Polyvinylpyrollidone, Gelatin, Corn starch', Magnesium Stearate, Microcrystalline Cellulose, Polyethylene glycol 6000,Sodium Benzoate ,Sodium Starch Glycolate, Stearic acid, Purified Talc, Titanium Dioxide, Yellow iron oxide.

PRINCIPAL DISPLAY PANEL - 50 Pouch Carton

NDC:68737-225-09

Compare to the Active Ingredients in
Tylenol®Allergy
Multi-Symptom*

ConRx
Allergy MULTI - SYMPTOM
Sinus

Sneezing - Runny Nose - Congestion

 

Principal Display Panel - 50 Pouch Carton
CONRX   ALLERGY SINUS MULTI-SYMPTOMS
acetaminophen, chlorpheniramine maleate, and phenylephrine hydrochloride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68737-225
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen325 mg
Chlorpheniramine maleate (UNII: V1Q0O9OJ9Z) (Chlorpheniramine - UNII:3U6IO1965U) Chlorpheniramine maleate2 mg
Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV) Phenylephrine Hydrochloride5 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
BIS(1-METHYLAMYL) SODIUM SULFOSUCCINATE (UNII: 772Y8KZU65)  
POVIDONE K90 (UNII: RDH86HJV5Z)  
GELATIN (UNII: 2G86QN327L)  
STARCH, CORN (UNII: O8232NY3SJ)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
Product Characteristics
ColorWHITEScore2 pieces
ShapeROUNDSize12mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68737-225-0950 in 1 BOX
12 in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34107/11/2012
Labeler - Eagle Distributors,Inc. (929837425)

Revised: 7/2012
Document Id: 2596b3d9-3b6c-4325-9a9d-dfe4bb3c3e91
Set id: 525ad077-ce4c-4354-be5d-d88a4abb3722
Version: 1
Effective Time: 20120710
 
Eagle Distributors,Inc.