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DELTUSS DP Nasal Decongestant Antihistamine CHERRY Flavor

Medically reviewed on August 28, 2017.

Dosage form: liquid
Ingredients: DEXCHLORPHENIRAMINE MALEATE 1mg in 5mL, PSEUDOEPHEDRINE HYDROCHLORIDE 30mg in 5mL
Labeler: Deliz Pharmaceutical Corp
NDC Code: 58238-226

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.

DELTUSS DP Nasal Decongestant Antihistamine CHERRY Flavor

Drug Facts


Active ingredients (in each 5 mL teaspoonful)

Dexchlorpheniramine maleate 1 mg
Pseudoephedrine HCl 30 mg

Purpose

Antihistamine

Nasal Decongestant

Uses
  • temporarily relieves nasal congestion due to the common cold, hay fever or other respiratory allergies
  • temporarily relieves runny nose, sneezing, itching of the nose or throat, and itchy, watery eyes due to hay fever (allergic rhinitis)
  • temporarily restores freer breathing through the nose

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 giving this product.

Ask a doctor before use if

you have

  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes
  • a breathing problem such as emphysema or chronic bronchitis
  • glaucoma
  • difficulty in urination due to enlarged prostrate gland

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.


When using this product
  • do not exceed recommended dosage
  • marked drowsiness may occur
  • alcohol, sedatives, and tranquilizers may increase the drowsiness effect
  • avoid alcoholic beverages
  • use caution when driving a motor vehicle or operating machinery
  • excitability may occur especially in children

Stop use and ask a doctor if
  • symptoms do not improve within 7 days or are accompanied by fever
  • nervousness, dizziness, or sleeplessness occur

If pregnant or breastfeeding

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
  • use only with enclosed measuring cup
  • do not use enclosed measuring cup for any other drug product
Adults and children 12 years of age and older:
2 teaspoonfuls (tsp) every 6 hours not to exceed 8 teaspoonfuls in 24 hours, or as directed by a doctor.
Children 6 to under 12 years of age:
1 teaspoonful (tsp) every 6 hours not to exceed 4 teaspoonfuls in 24 hours, or as directed by a doctor.
Children 2 to under 6 years of age:
Consult a doctor.

Other information
  • Store at room temperature 15°C-30°C (59°F-86°F)

Inactive ingredients

cherry flavor, citric acid, glycerin, propylene glycol, purified water, sodium citrate, sodium saccharin, sorbitol

Questions?

Call 1-787-701-3312. You may also report serious side effects to this phone number.

DELTUSS DP Nasal Decongestant Antihistamine CHERRY Flavor 4oz/118ml (58238-226-04)

DELTUSS DP NASAL DECONGESTANT ANTIHISTAMINE CHERRY FLAVOR 
dexchlorpheniramine maleate, pseudoephedrine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58238-226
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXCHLORPHENIRAMINE MALEATE (DEXCHLORPHENIRAMINE) DEXCHLORPHENIRAMINE MALEATE1 mg  in 5 mL
PSEUDOEPHEDRINE HYDROCHLORIDE (PSEUDOEPHEDRINE) PSEUDOEPHEDRINE HYDROCHLORIDE30 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE 
GLYCERIN 
PROPYLENE GLYCOL 
WATER 
SODIUM CITRATE 
SACCHARIN SODIUM 
SORBITOL 
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRY (Cherry Flavor) Imprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:58238-226-041 BOTTLE in 1 PACKAGE
1118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34103/20/2015
Labeler - Deliz Pharmaceutical Corp (826391138)
Establishment
NameAddressID/FEIOperations
Woodfield Pharmaceutical, LLC079398730manufacture(58238-226)

 
Deliz Pharmaceutical Corp

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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