Active Ingredient (In Each 10 Ml)
Guaifenesin, USP 200 mg
The following Structured Product Label (SPL) was submitted to the FDA by Central Texas Community Health Centers for the product Sunmark Tussin (NDC 76413-328). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each 10 ml), purpose, use, ask a doctor before use if you have, stop use and ask a doctor if, if pregnant or breast-feeding,, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Guaifenesin, USP 200 mg
Expectorant
helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive
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.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
age | dose |
adults and children 12 years and over | 10 – 20 mL every 4 hours |
children under 12 years | do not use |
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
1-800-719-9260
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.
* Please review the disclaimer below.