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

Country: United States

Language: English

Source: NLM (National Library of Medicine)

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Active ingredient:

DEXCHLORPHENIRAMINE MALEATE (UNII: B10YD955QW) (DEXCHLORPHENIRAMINE - UNII:3Q9Q0B929N), PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F)

Available from:

Deliz Pharmaceutical Corp

INN (International Name):

DEXCHLORPHENIRAMINE MALEATE

Composition:

DEXCHLORPHENIRAMINE MALEATE 1 mg in 5 mL

Administration route:

ORAL

Prescription type:

OTC DRUG

Therapeutic indications:

- 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

Authorization status:

OTC monograph final

Summary of Product characteristics

                                DELTUSS DP NASAL DECONGESTANT ANTIHISTAMINE CHERRY FLAVOR-
DEXCHLORPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE LIQUID
DELIZ PHARMACEUTICAL CORP
_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._
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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.
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