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FDA LABEL GENERIC: Dexbrompheniramine MFR: Poly Pharmaceuticals, Inc.

Dexbrompheniramine Maleate 0.2 Mg/ml / Dextromethorphan Hydrobromide 2 Mg/ml / Pseudoephedrine Hydrochloride 6 Mg/ml Oral Solution

(in each 5 mL teaspoonful)

Dexbrompheniramine Maleate 1 mg

Dextromethorphan Hydrobromide 10 mg

Pseudoephedrine Hydrochloride 30 mg

Antihistamine
Antitussive
Nasal Decongestant

INDICATIONS AND USAGE

temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:

runny nose
sneezing
itching of nose or throat
itchy, watery eyes
cough due to minor throat and bronchial irritation
nasal congestion
reduces swelling of nasal passages

WARNINGS

Do not exceed recommended dosage. 

this product

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.

if you have

a breathing problem such as emphysema or chronic bronchitis
glaucoma
trouble urinating due to an enlarged prostate gland
a cough that lasts or is chronic such as occurs with smoking, asthma or emphysema
a cough that occurs with too much phlegm (mucus)
heart disease
high blood pressure
thyroid disease
diabetes

if you are

taking sedatives or tranquilizers.

excitability may occur, especially in children
may cause marked drowsiness
avoid alcoholic drinks
alcohol, sedatives, and tranquilizers may increase the drowsiness effect
be careful when driving a motor vehicle or operating machinery
nervousness, dizziness, or sleeplessness occur
cough or nasal congestion persists for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache. A persistent cough may be a sign of a serious condition.
new symptoms occur

ask a health professional before use.

In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE AND ADMINISTRATION

Do not exceed recommended dosage.

Adults and

children 12

years of age

and over:
2 teaspoonful (10 mL)

every 4 to 6 hours,

not to exceed 8

teaspoonfuls in a 24

hours
Children 6 to

under 12 years

of age:
1 teaspoonful

(5 mL) every 4 to 6

hours, not to exceed

4 teaspoonfuls in 24 hours
Children under

6 years of age:
Consult a doctor.

Store at 59° - 86°F (15° - 30°C)

Citric acid, flavors, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol solution, sucralose.

Serious side effects associated with use of this product may be reported to this number.
Call 1-800-882-1041
Mon. - Fri. (8 a.m. to 5 p.m. CST).

ASK A DOCTOR

NDC 50991-142 -16


Duratuss DM

LIQUID

Antihistamine • Antitussive

Nasal Decongestant

Raspberry Bubble Gum Flavor

SUGAR FREE / ALCOHOL FREE

DYE FREE / GLUTEN FREE

16 fl oz. (473 mL)


Tamper evident by foil seal under cap. Do not use if foil seal is broken or missing.
Dispense in a tight, light-resistant container with a child-resistant cap.
THIS BOTTLE IS NOT TO BE DISPENSED TO CONSUMER.
Distributed by: Poly Pharmaceuticals, Owens Cross Roads, AL 35763