ALLFEN DM - guaifenesin and dextromethorphan hydrobromide tablet 
MCR American 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
(in each immediate-release tablet)
Purpose
Dextromethorphan HBr 20 mgAntitussive
Guaifenesin 400 mgExpectorant

Uses

temporarily relieves

Warnings

  • 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 use this product unless directed by a doctor

  • 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
  • for persistent or chronic cough such as occurs with smoking, asthma, or emphysema, or if cough is accompanied by excessive phlegm (mucus)

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

Keep out of reach of children.

In case of accidental overdose, seek professional help or contact a Poison Control Center immediately.

Directions

Do not exceed recommended dosage.

Adults and children 12 years of age and over:1 tablet every 4 hours, not to exceed 6 tablets in 24 hours, or as directed by a doctor
Children 6 to under 12 years of age:1/2 tablet every 4 hours, not to exceed 3 tablets in 24 hours, or as directed by a doctor
Children 2 to under 6 years of age:Consult a doctor

Inactive Ingredients

Magnesium Stearate, Microcrystalline Cellulose, Sodium Starch Glycolate

Question? Comments?

Call 1-352-754-8587

PRINCIPAL DISPLAY PANEL - 100 Tablet Bottle Label

NDC 58605-0401-01

100 tablets

Allfen DM

Antitussive • Expectorant

Each immediate-release tablet contains:
Dextromethorphan HBr20 mg
Guaifenesin400 mg

MCR American

Principal Display Panel - 100 Tablet Bottle Label

ALLFEN DM 
guaifenesin and dextromethorphan hydrobromide tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58605-401
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (GUAIFENESIN) GUAIFENESIN400 mg
Dextromethorphan Hydrobromide (Dextromethorphan) Dextromethorphan Hydrobromide20 mg
Inactive Ingredients
Ingredient NameStrength
Magnesium Stearate 
Cellulose, Microcrystalline 
Sodium Starch Glycolate Type A Potato 
Product Characteristics
ColorWHITEScore2 pieces
ShapeOVAL (Capsule Shaped) Size16mm
FlavorImprint Code ALLFEN;DM
Contains    
Packaging
#Item CodePackage DescriptionMultilevel Packaging
1NDC:58605-401-01100 TABLET ( TABLET) in 1 BOTTLE, PLASTICNone
2NDC:58605-401-0220 TABLET ( TABLET) in 1 BLISTER PACKNone

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34103/31/2008

Labeler - MCR American Pharmaceuticals, Inc. (783383011)
Establishment
NameAddressID/FEIOperations
MCR American Pharmaceuticals, Inc.783383011MANUFACTURE

Revised: 05/2011 MCR American Pharmaceuticals, Inc.