ACTIDOM DMX- dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride solution 
ACTIPHARMA, LLC

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ACTIDOM DMX

Drug Facts

Active ingredients (in each 5 mL tsp)

Dextromethorphan HBr, 30 mg
Guaifenesin, 200 mg
Phenylephrine HCl, 10 mg

Purposes

Cough suppressant
Expectorant
Nasal decongestant

Uses

• Helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
• Temporarily relieves these symptoms occurring with a cold:
• nasal congestion • cough due to minor throat and bronchial irritation.

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 your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have • heart disease • high blood pressure • thyroid disease • diabetes • trouble urinating due to an enlarged prostate gland • cough that occurs with too much phlegm (mucus) • cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema.

Ask a doctor or pharmacist before use if you are taking any other oral nasal decongestant or stimulant.

When using this product • do not exceed recommended dosage

Stop use and ask a doctor if
• you get nervous, dizzy or sleepless 
• symptoms do not get better within 7 days or are accompanied by fever
• coughs lasts more than 7 days, comes back, or is accompanied by fever, rash, or a persistent headache. These could be signs of a serious condition.

If pregnant or breast-feeding, 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.

Directions

  • do not take more than 4 doses in any 24-hour period.

AGEDOSE

Adults and Children 12 years

of age and over 

 Take 1 teaspoonfuls

(5 mL) every 6 hours

 Children under 12 years of

   age

ask a doctor 

Other information

• Tamper Evident Feature: Do not use if safety seal is torn, cut or opened.
• Store at controlled room temperature 15° - 30ºC (59º - 86ºF).
• Avoid excessive heat or humidity.

Inactive ingredients

Citric acid, D&C Red #40, FD&C Blue #1, flavor, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium citrate, sucralose.

Questions or comments?

call weekdays from 8AM to 4PM AST at 1.787.608.0882

Contains the same active ingredients as Dometuss®-DMX*

SUGAR FREE

ALCOHOL FREE

Grape Flavor

Manufactured in USA with imported ingredients for ActiPharma. San Juan, PR 00917. www.actipharma.net.

* Dometuss® DMX is a registered trademark of Domel Laboratories. This product is not manufactured, distributed or marketed by Domel Laboratories.

Packaging

Actidom DMX

ACTIDOM DMX 
dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63102-110
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE30 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg  in 5 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
Colorpurple (Clear) Score    
ShapeSize
FlavorgrapeImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63102-110-16474 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/13/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01208/13/2015
Labeler - ACTIPHARMA, LLC (079340948)

Revised: 6/2024
Document Id: 07838a85-4ddc-470d-a344-001587f2d904
Set id: 0166322e-7dbb-4658-a5c5-1d0525bb7655
Version: 4
Effective Time: 20240628
 
ACTIPHARMA, LLC