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Glentuss

Dosage form
SYRUP
Labeler
Glendale Inc
Label updated
2015-12-09
Retrieved
2026-09-07
Active ingredients
DEXTROMETHORPHAN HYDROBROMIDE · DOXYLAMINE SUCCINATE · PSEUDOEPHEDRINE HYDROCHLORIDE
View original label and images on DailyMed ↗
Label information

Drug Facts

유효 성분

성분·작용

Active ingredients (in each teaspoonful) Purpose
Dextromethorphan Hydrobromide 15 mg Antitussive (cough suppressant)
Pseudoephedrine Hydrochloride 30 mg Nasal Decongestant
Doxylamine Succinate 6.25 mg Antihistamine
Uses

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

  • cough due to minor throat and bronchial irritation
  • runny nose
  • sneezing
  • itching of the nose or throat
  • itchy, watery eyes
  • nasal congestion
  • temporarily restores freer breathing through the nose congestion
  • reduces swelling of nasal passages
Warnings

Do not exceed recommended dosage.

Do not use this product

  • to sedate a child or make a child sleepy
  • 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
  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • a breathing problem such as emphysema or chronic bronchitis
  • a cough that lasts or is chronic such as occurs with smoking, asthma or emphysema
  • a cough that occur with too much phlegm (mucus)

Ask a doctor or pharmacist before use if you are

  • taking any other nasal decongestant or stimulant
  • taking sedatives or tranquilizers

When using this product

  • marked drowsiness may occur
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery
  • excitability may occur, especially in children

Stop use and ask a doctor if

  • 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. These could be signs of a serious condition.

Label information

If pregnant or breast-feeding, ask a health professional before use.

Label information

Keep out of reach of children.

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

Directions

Do not exceed 4 dosage in a 24-hour period.

Adults and children 12 years of age and over: 2 teaspoonfuls every 6 hours
Children under 12 years of age: Consult a physician
Other information

Store at 59°-86°F (15°-30°C) [see USP for Controlled Room Temperature]

Inactive ingredients

Apple candy flavor, citric acid, glycerin, propylene glycol, purified water, saccharin sodium, sodium benzoate, sorbitol.

Questions? Comments?

To report a serious adverse event or obtain product information, Call 1-630-530-7000.

Label information

Distributed by:
Glendale Inc
Villa, Park, IL 60181

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

NDC 70147-0233-16

Glentuss

Antitussive
Nasal Decongestant
Antihistamine

Each teaspoonful for oral
administration contains:

Dextromethorphan HBr 15 mg
Pseudoephedrine HCl 30 mg
Doxylamine Succinate 6.25 mg

SUGAR FREE / DYE FREE
ALCOHOL FREE

Apple Candy Flavored Liquid

Tamper evident by foil seal under cap.
Do not use if foil seal is broken or missing.

Distributed by:
Glendale Inc
Villa Park, IL 60181

16 fl oz. (473 mL)

[Image in the official label — see DailyMed source]

DailyMed Set ID: 8a6eb670-8bed-4941-b4fd-70b3f1e48401 · Version 1
NDC: 70147-233