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ACTIDOM DMX

Medically reviewed on Oct 16, 2018

Dosage form: solution
Ingredients: DEXTROMETHORPHAN HYDROBROMIDE 30mg in 5mL, GUAIFENESIN 200mg in 5mL, PHENYLEPHRINE HYDROCHLORIDE 10mg in 5mL
Labeler: Actipharma, Inc
NDC Code: 63102-110

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.

ACTIDOM DMX

Drug Facts

Drug Facts

Active Ingredients (in each 5 mL tsp)

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

Purpose

Cough Suppressant

Expectorant

Nasal Decongestant

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

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 • diabetes • heart disease • thyroid disease • high blood pressure • 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.

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.

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

 Adults and Children 12 years of age and over          5 mL (1tsp), every 6 hours
 Children under 12 years of age                                            ask a doctor

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

Other information • Store at room temperature 15° - 30ºC (59º - 86ºF) • protect from freezing • protect from light • Avoid excessive heat or humidity. TAMPER EVIDENT: Do not use if inner seal is torn, broken or missing.

Manufactured in the USA for ActiPharma, Inc. Dorado, PR 00646. Tel: (787)608-0882

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

Contains the same active ingredients as Dometuss®-DMX*

COUGH SUPPRESSANT

EXPECTORANT

NASAL DECONGESTANT

SUGAR FREE

ALCOHOL FREE

Grape Flavor

Packaging

ACTIDOM DMX 
dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63102-110
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE30 mg  in 5 mL
GUAIFENESIN (GUAIFENESIN) GUAIFENESIN200 mg  in 5 mL
PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINE) PHENYLEPHRINE HYDROCHLORIDE10 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE 
FD&C RED NO. 40 
FD&C BLUE NO. 1 
GLYCERIN 
METHYLPARABEN 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
SODIUM CITRATE 
SUCRALOSE 
Product Characteristics
Colorpurple (Clear) Score    
ShapeSize
FlavorgrapeImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:63102-110-16474 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34108/13/2015
Labeler - Actipharma, Inc (079340948)

 
Actipharma, Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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