ACTINEL- dextromethorphan hbr,guaifenesin,pseudoephedrine hcl solution 
Actipharma, Inc

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ACTINEL®

​Drug Facts

Active Ingredients (in each 5 mL tsp)

Dextromethorphan HBr, 15 mg
Guaifenesin, 200 mg
Pseudoephedrine HCl, 30 mg

Purposes

Cough Suppressant
Expectorant
Nasal Decongestant

​Uses

• temporarily relieves cough due to minor throat and bronchial irritation associated with the common cold • helps control the cough reflex that causes coughing • helps loosen phlegm (mucus) and thin bronchial secretions to make cough more productive • temporarily relieves nasal congestion due to the common cold, hay fever, or other upper respiratory allergies (allergic rhinitis).

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 use more than directed.

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
• cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or 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 2 teaspoonfuls
(10 mL) every 6 hours
 Children under 12 years of
age
 do not use

Other information

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

Inactive ingredients

Citric Acid, Flavor, Methylparaben, Potassium Citrate, Propylene Glycol, Propylparaben, Purified Water, Sorbitol, Sucralose

Questions or comments?

call weekdays from 8AM to 4PM AST at 1.787.608.0882

NEW FORMULA

Contains the same active ingredients as Tusnel®*

SUGAR FREE
DYE FREE
ALCOHOL FREE
SACCHARIN FREE

COMMITTED TO HEALTH AND WELL-BEING
WWW.ACTIPHARMA.NET 

Manufactured in USA with imported ingredients for ActiPharma, Inc.
San Juan, PR 00917.

* Tusnel® is a registered trademark of Llorens Pharmaceutical Corp. This product is not manufactured, distributed or marketed by Llorens Pharmaceutical Corp.

Packaging

ACTINEL-101

ACTINEL 
dextromethorphan hbr,guaifenesin,pseudoephedrine hcl solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63102-101
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) GUAIFENESIN200 mg  in 5 mL
PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE30 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63102-101-16474 mL in 1 BOTTLE; Type 0: Not a Combination Product09/24/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01209/24/2014
Labeler - Actipharma, Inc (079340948)

Revised: 10/2023
Document Id: 7ffd904d-64c8-4328-bd53-7a99f3c535b4
Set id: db0cb6ae-0a4d-4232-805a-f3f3a058261f
Version: 4
Effective Time: 20231004
 
Actipharma, Inc