RX ACT TUSSIN COUGH- dextromethorphan hydrobromide liquid
H E B

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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HEB Tussin Drug Facts

Active ingredient (in each 5 mL tsp)

Dextromethorphan HBr, USP 15 mg

Purpose

Cough suppressant

Use

•: 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

Stop use and ask a doctor if

cough lasts for more than 7 days, comes back, or occurs with 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.

Directions

•: do not take more than 4 doses in any 24-hour period
•: this adult product is not intended for use in children under 12 years of age

age

dose

children under 12 years

do not use

adults and children

12 years and over

2 teaspoons

every 6 to 8 hours

Other information

•: store at 20°-25°C (68°-77°F)

Inactive ingredients

alcohol, anhydrous citric acid, FD&C red no. 40, flavors, glycerin, high fructose corn syrup, purified water, saccharin sodium, sodium benzoate

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to Robitussin® Cough Long-Acting active ingredient

TUSSIN

Cough

Dextromethorphan HBr (Cough Suppressant)

Long-Acting

Non-Drowsy

Relieves:

Cough up to 8 Hours

Adult

For Ages 12 & Over

ALCOHOL 1.4%

GLUTEN FREE

Tussin Carton Image 1

Tussin Carton Image 2

RX ACT TUSSIN COUGH
dextromethorphan hydrobromide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:37808-300
Route of Administration	ORAL

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

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

Product Characteristics
Color	RED	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:37808-300-34	1 in 1 CARTON	05/05/1992	08/22/2015
1		237 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part341	05/05/1992	08/22/2015

Labeler - H E B (007924756)

Revised: 11/2017

Document Id: 50aee93b-d2e3-4722-8a95-30dc630a7556

Set id: 7bdbc577-8cc9-48f6-b2da-92d274080b05

Version: 3

Effective Time: 20171119

H E B