TUSSIN LONG ACTING COUGH- dextromethorphan hbr liquid

Tussin Long Acting Cough by

Drug Labeling and Warnings

Tussin Long Acting Cough by is a Otc medication manufactured, distributed, or labeled by Chain Drug Consortium, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each 5 mL, 1 teaspoon)

Dextromethorphan HBr, USP 15 mg

Purpose

Cough suppressant

Uses

• temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold

Warnings

Do not use

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

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

When using this product,

• do not use more than directed

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 (1-800-222-1222) immediately.

Directions

• do not exceed 4 doses in a 24-hour period
• this adult product is not intended for use in children under 12 years of age
• use enclosed dosage cup
• tsp = teaspoon, mL = milliliter

• age: dose
• adults and children 12 years and over: 2 teaspoons (10 mL) every 6-8 hours
• children under 12 years: do not use

Other information

• store at room temperature

Inactive ingredients

alcohol, citric acid, FD&C red 40, flavor, glucose, glycerin, high fructose corn syrup, menthol, purified water, saccharin sodium, sodium benzoate

Questions or comments?

1-866-534-4631

Principal Display Panel

Compare to active ingredient in Robitussin® Lingering Cold Long-Acting Cough*

Tussin Long-acting Cough

Dextromethorphan HBr

Cough suppressant

Cough formula for adults

Alcohol 1.4%

FL OZ (mL)

*This product is not manufactured or distributed by Wyeth Consumer Healthcare, distributors of Robitussin® Lingering Cold Long-Acting Cough.

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL ON THE BOTTLE IS BROKEN OR MISSING.

PARENTS: Learn about teen medicine abuse   www.StopMedicineAbuse.org

DISTRIBUTED BY

CHAIN DRUG CONSORTIUM

3301 NW BOCA RATON BLVD

SUITE 101, BOCA RATON, FL 33431

MADE IN USA

Package Label

Premier Value Tussin Long-acting Cough Liquid

INGREDIENTS AND APPEARANCE

TUSSIN LONG ACTING COUGH 
dextromethorphan hbr liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68016-098
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	15 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C RED NO. 40 (UNII: WZB9127XOA)
DEXTROSE (UNII: IY9XDZ35W2)
GLYCERIN (UNII: PDC6A3C0OX)
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
MENTHOL (UNII: L7T10EIP3A)
WATER (UNII: 059QF0KO0R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68016-098-04	1 in 1 BOX	01/29/2013	12/31/2020
1		118 mL in 1 BOTTLE, PLASTIC; 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	01/29/2013	12/31/2020

Labeler - Chain Drug Consortium, LLC (101668460)