GUAIFENESIN PHENYLEPHRINE DEXTROMETHORPHAN- guaifenesin, phenylephrine hcl, dextromethorphan tablet, coated 
Kramer Novis.

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 (In Each Tablet)                       
Guaifenesein    400 mg
Phenylephrine HCl 10 mg
Dextromethorphan HBr. 20 mg

Expectorant, nasal decongestant, antitussive (anti cough)

Uses: temporarily relieves these symptoms occurring with a cold

nasal decongestion: cough due to minor throat and bronchial irritation

•    helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

Directions:
Adults and children 12 years of age and older
•    Take 1 tablet every 4 hours as needed, do not exceed 6  
tablets in 24 hours, or as directed by a doctor.
•    Children under 12 years, consult a doctor
•    Warnings:

Warnings:
•    when using this product do not exceed recommended dose.
•    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 MAOI drug. If you do not know if your prescription  
drug contains an MAOI, consult a doctor or pharmacist before  
taking this product
Stop use and ask a doctor if:
•    symptoms do not improve
•    new symptoms occur
•    redness or swelling is present
•    nervousness, dizziness or sleeplessness occur
•    symptoms do not improve within 7 days or are accompanied by  
fever
•    cough persists for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition
Ask a doctor before use if you have:
•    heart disease
•    high blood pressure
•    thyroid disease
•    diabetes
•    difficulty in urination due to enlargement of the prostate gland
•    persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema or where cough is accompanied by excessive phlegm (mucus)

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

KEEP OUT OF REACH OF CHILDREN. In case of overdose,  
get medical help or contact a Poison Control 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.

Inactive Ingredients: Hypromellose,  Microcrystalline Cellulose, Polydextrose, Polyethylene Glycol,  Povidone,  Sodium Starch Glycolate, Stearic Acid


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GUAIFENESIN PHENYLEPHRINE DEXTROMETHORPHAN 
guaifenesin, phenylephrine hcl, dextromethorphan tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52083-249
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYDEXTROSE (UNII: VH2XOU12IE)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
POVIDONE K30 (UNII: U725QWY32X)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite (snow white) Score2 pieces
ShapeCAPSULE (T) Size19mm
FlavorImprint Code T
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52083-249-022 in 1 PACKET; Type 0: Not a Combination Product07/18/201211/30/2018
2NDC:52083-249-6060 in 1 BOTTLE; Type 0: Not a Combination Product07/18/201211/30/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34107/18/201211/30/2018
Labeler - Kramer Novis. (090158395)
Registrant - Ultraseal Corporation (085752004)
Establishment
NameAddressID/FEIBusiness Operations
Ultratab Laboratories, Inc.151051757manufacture(52083-249)

Revised: 11/2018
 
Kramer Novis.