Q-Tussin

Dosage form: solution
Ingredients: GUAIFENESIN 100mg in 5mL
Labeler: Preferred Pharmaceuticals, Inc
NDC code: 68788-9081

Medically reviewed by Drugs.com. Last updated on Nov 20, 2023.

Q-Tussin 0857

Active ingredient (in each 5 mL = 1 tsp)

Guaifenesin, USP 100 mg

Purpose

Expectorant

Use

helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive

Warnings

Ask a doctor before use if you have

•: cough that occurs with too much phlegm (mucus)
•: cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema

Stop use and ask a doctor if cough lasts more than 7 days, comes back or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

If pregnant or breast-feeding, 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

•: do not take more than 6 doses in any 24-hour period
•: this adult product is not intended for use in children under 12 years of age

age (yr)	dose (tsp)
adults and children 12 years and over	2 - 4 teaspoons every 4 hours
children under 12 years	do not use

Other information

•: each tsp contains: sodium 2 mg
•: store at 15° to 30°C (59° to 86°F)
•: dosage cup provided

You may report serious side effects to: 130 Vintage Drive, Huntsville, AL 35811.

Inactive ingredients

caramel color, FD&C red #40, flavor, glycerin, liquid glucose, purified water, saccharin sodium, sodium benzoate

Made in the USA
for Qualitest Pharmaceuticals
Huntsville, AL 35811

Rev. 5/09 R7
8273611 0857

Relabeled By: Preferred Pharmaceuticals Inc.

PRINCIPAL DISPLAY PANEL

Q-TUSSIN
guaifenesin solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:68788-9081(NDC:0603-0857)
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GUAIFENESIN (GUAIFENESIN)	GUAIFENESIN	100 mg in 5 mL

Inactive Ingredients
Ingredient Name	Strength
CARAMEL
FD&C RED NO. 40
GLYCERIN
GLUCOSE OXIDASE
WATER
SACCHARIN SODIUM
SODIUM BENZOATE

Product Characteristics
Color	ORANGE (clear, reddish-orange)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description
1	NDC:68788-9081-1	118 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	10/01/1997

Labeler - Preferred Pharmaceuticals, Inc (791119022)

Registrant - Preferred Pharmaceuticals, Inc (791119022)

Establishment
Name	Address	ID/FEI	Operations
Preferred Pharmaceuticals, Inc		791119022	RELABEL(68788-9081)

Document Id: 10360f95-ef8e-4279-9c46-31708c8bf7d9

Set id: 36231ec1-97c0-4931-a689-ac74268a6bb7

Version: 5

Effective Time: 20171129

Preferred Pharmaceuticals, Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer