DELTUSS DP NASAL DECONGESTANT ANTIHISTAMINE CHERRY FLAVOR- dexchlorpheniramine maleate, pseudoephedrine hydrochloride liquid

DELTUSS DP Nasal Decongestant Antihistamine CHERRY Flavor by

Drug Labeling and Warnings

DELTUSS DP Nasal Decongestant Antihistamine CHERRY Flavor by is a Otc medication manufactured, distributed, or labeled by Deliz Pharmaceutical Corp, Woodfield Pharmaceutical, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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)

INGREDIENTS AND APPEARANCE

DELTUSS DP NASAL DECONGESTANT ANTIHISTAMINE CHERRY FLAVOR 
dexchlorpheniramine maleate, pseudoephedrine hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58238-226
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXCHLORPHENIRAMINE MALEATE (UNII: B10YD955QW) (DEXCHLORPHENIRAMINE - UNII:3Q9Q0B929N)	DEXCHLORPHENIRAMINE MALEATE	1 mg  in 5 mL
PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F)	PSEUDOEPHEDRINE HYDROCHLORIDE	30 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHERRY (Cherry Flavor)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58238-226-04	1 in 1 PACKAGE	03/20/2015
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	03/20/2015

Labeler - Deliz Pharmaceutical Corp (826391138)

Establishment
Name	Address	ID/FEI	Business Operations
Woodfield Pharmaceutical, LLC		079398730	manufacture(58238-226)