DURAFLU- acetaminophen, dextromethorphan hbr, guaifenesin, pseudoephedrine hcl tablet, film coated 
Poly Pharmaceuticals, 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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Drug Facts

Active Ingredients

Acetaminophen 500 mg
Dextromethorphan HBr 20 mg                                                                               
Guaifenesin 200 mg
Pseudoephedrine HCl 60 mg                                                                                

Purpose

Pain reliever
Antitussive
Expectorant
Nasal decongestant

Uses

Acetaminophen is an analgesic (pain reliever) and antipyretic (fever reducer).  Dextromethorphan temporarily suppresses cough due to minor bronchial irritation associated with a cold or inhaled irritants. Guaifenesin is an expectorant that helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes. Pseudoephedrine is a nasal decongestant, for the temporary relief of nasal congestion due to the common cold.

Warnings

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

  • more than FOUR tablets 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.

Ask doctor before use

if you have liver disease

Ask a doctor or a pharmacist before use

if you are taking the blood thinning drug warfarin.

If you are pregnant or nursing consult a doctor before using this product.

Stop use and ask a doctor if

  • pain, cough, 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
  • cough comes back or occurs with rash or headache that lasts

When using this product

a persistent cough may be a sign of a serious condition. If cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache, consult a doctor.  Do not take this product for persistent or chronic cough such as occurs with smoking, asthma, or emphysema, or if cough is accompanied by excessive phlegm (mucus) unless directed by a doctor.

Do not exceed recommended dosage.  

If nervousness, dizziness, or sleeplessness occur, discontinue use and consult a doctor.  If symptoms do not improve within 7 days or are accompanied by fever, consult a doctor.  Do not take this product if you have heart disease, high blood pressure, thyroid disease, diabetes, or difficulty in urination due to enlargement of the prostate gland unless directed by a doctor.

Drug Interaction Precaution.  

Do not use this product 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 are uncertain whether your prescription drug contains an MAOI, consult a health professional before taking this product.

Keep out of reach of children

  • ​If swallowed, immediately call Poison Control Center or doctor.

Directions

Dose as follows or as directed by a doctor.

Adults and Children over 12 Years of age: one tablet four times per day not to exceed 4 tablets in 24 hours. Children 6 to 12 years of age: 1/2 tablet every 4 hours, not to exceed 2 tablets in 24 hours. Children under 6 years of age: Consult a physician.

Other information

Store at 20°-25°C (68°-77°F) as defined in the (USP/NF). Dispense in tight, light-resistant container.

Supplied in 100ct bottle, NDC 50991-0510-01.

CAUTION: Under Federal DEA law a retail outlet must store this product out of reach of customers.

Inactive ingredients

Hypromellose, Magnesium Stearate, Microcrystalline Cellulose, Modified Cellulose Gum, Silicon Dioxide, Starch, Stearic Acid.

Questions or comments?

800-882-1041

Manufactured For:
Poly Pharmaceuticals, Inc.
Quitman, MS 39355

Rev. 10/12

Principal Display Panel

NDC 50991-0510-01
DURAFLU
Expectorant/ Nasal Decongestant
Antitussive/Pain Reliever
100 Tablets

NDC 50991-0510-01 DURAFLU™ Expectorant/ Nasal Decongestant Antitussive/Pain Reliever 100 Tablets
DURAFLU 
acetaminophen, dextromethorphan hbr, guaifenesin, pseudoephedrine hcl tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50991-510
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg
PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE60 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize20mm
FlavorImprint Code PE;723
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50991-510-0212 in 1 CARTON02/10/201112/01/2016
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:50991-510-01100 in 1 BOTTLE; Type 0: Not a Combination Product02/10/201112/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34102/10/201112/01/2016
Labeler - Poly Pharmaceuticals, Inc. (198449894)

Revised: 4/2014
 
Poly Pharmaceuticals, Inc.