sunmark tussin
- Dosage form
- SOLUTION
- Labeler
- Central Texas Community Health Centers
- Label updated
- 2016-12-09
- Retrieved
- 2026-09-07
- Active ingredients
- GUAIFENESIN
Active ingredient (in each 10 mL)
Guaifenesin, USP 200 mg
Purpose
Expectorant
Use
helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive
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 for more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. A persistent cough may be a sign 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 (1-800-222-1222).
Directions
-
• do not take more than 6 doses in any 24-hour period -
• measure only with dosing cup provided -
• keep dosing cup with product -
• mL = milliliter -
• this adult product is not intended for use in children under 12 years of age
|
age |
dose |
|
adults and children 12 years and over |
10 – 20 mL every 4 hours |
|
children under 12 years |
do not use |
Other information
-
• store at 20-25°C (68-77°F). Do not refrigerate.
Inactive ingredients
anhydrous citric acid, caramel, FD&C red no. 40, flavor, glycerin, high fructose corn syrup, maltol, menthol, propylene glycol, purified water, saccharin sodium, sodium benzoate
Questions or comments?
1-800-719-9260
PRINCIPAL DISPLAY PANEL - 118 mL Bottle Carton Label
CommUnityCare Federally Qualified Health Centers
TUSSIN
118ml
Date:
Dr.
Name:
TAKE AS DIRECTED.
123456
1/1/01
TUSSIN 118ml NDC 76413-328-01
Batch: 123456
Lot: 123456
Exp: 1/1/01
SUNMARK
Federal law prohibits the transfer of this drug to any other person than the patient for whom prescribed.
[Image in the official label — see DailyMed source]
DailyMed Set ID: 7b1492ef-c8ab-4776-97b1-5982d2ea69a0 · Version 1
NDC: 76413-328