BIODESP  DM- dextromethorphan, guaifenesin, phenylephrine liquid 
Advanced Generic Corporation

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 5 mL tsp.)              Purpose

Dextromethorphan Hydrobromide 15 mg.................. Cough Suppressant

Guaifenesin 100 mg .............................................. Expectorant

Phenylephrine HCl 5 mg.................................. Decongestant

Purpose

Cough Suppressant

Expectorant

Nasal Decongestant

Uses

Warnings

Do not use

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 you are taking a prescription drug that contains an MAOI; ask your doctor or pharmacist before taking this product.

When using this product do not exceed recommended dosage

Ask a doctore before use if you have

Stop use and ask a doctor if

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

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

Directions Do not exceed 4 doses in 24 hours.

 adults and children 12 years of age and overtake 2 teaspoonfuls (10 mL) every 6 hours 
children 6 to under 12 years of age take 1 teaspoonful (5 mL) every 6 hours 
children 2 to under 6 years of age take 1/2 teaspoonful (2.5 mL) every 6 hours 
children under 2 years of age ask a doctor 

Questions or comments? 1-305-403-3788
Manufactured For: Advanced Generic Corporation, Miami, FL 33147.
www.advancedgeneric.com

Inactive ingredients artificial flavor, citric acid, methylparaben, propylene glycol,
propylparaben, purified water, sodium citrate and sucralose.

BiodespDMLabel

BIODESP   DM
dextromethorphan, guaifenesin, phenylephrine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45737-221
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS) Dextromethorphan Hydrobromide15 mg  in 5 mL
Guaifenesin (UNII: 495W7451VQ) (Guaifenesin - UNII:495W7451VQ) Guaifenesin100 mg  in 5 mL
Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV) Phenylephrine Hydrochloride5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
Water (UNII: 059QF0KO0R)  
Methylparaben (UNII: A2I8C7HI9T)  
Propylparaben (UNII: Z8IX2SC1OH)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Sodium Citrate (UNII: 1Q73Q2JULR)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPE (Grape Flavor) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:45737-221-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34101/01/2009
Labeler - Advanced Generic Corporation (831762971)

Revised: 12/2020
Document Id: fe676580-acff-42f8-bc7a-076af73dd1b4
Set id: 6b303f1a-0a8b-43a9-bb31-d5a0d46becc7
Version: 4
Effective Time: 20201223
 
Advanced Generic Corporation