Label: TUSSIN ADULT CHEST CONGESTION- guaifenesin syrup
- NDC Code(s): 59779-650-26, 59779-650-34
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
If you are a consumer or patient please visit this version.
- Active ingredient (in each 10 mL)
Guaifenesin, USP 200 mgClose
helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productiveClose
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.
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).
- 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
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 benzoateClose
- Questions or comments?
- Principal Display Panel
Compare to the active ingredient in Robitussin® Mucus + Chest Congestion
Adult Chest Congestion
For ages 12 & over
Dosage cup provided
8 FL OZ (237 mL)Close
- INGREDIENTS AND APPEARANCE
TUSSIN ADULT CHEST CONGESTION
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-650 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg in 10 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) CARAMEL (UNII: T9D99G2B1R) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) MALTOL (UNII: 3A9RD92BS4) MENTHOL (UNII: L7T10EIP3A) SACCHARIN SODIUM (UNII: SB8ZUX40TY) Product Characteristics Color RED (dark) Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-650-26 1 in 1 CARTON 1 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:59779-650-34 1 in 1 CARTON 2 237 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 07/15/1987 Labeler - CVS Pharmacy (062312574)