ADULT TUSSIN COUGH - dextromethorphan hydrobromide liquid 
H E B

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HEB Adult Tussin Cough Drug Facts

Active ingredient (in each 5 mL tsp)

Dextromethorphan HBr, USP 15 mg

Purpose

Cough suppressant

Uses

Warnings

Do not use

Ask a doctor before use if you have

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

agedose
children under 12 yearsdo not use

adults and children

12 years and over

2 teaspoons

every 6 to 8 hours

Other information

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

See New Dosing Directions

Compare to Adult Robitussin® Cough Long-Acting active ingredient

Adult

Tussin

Cough

Long-Acting

Non-Drowsy

Cough Suppressant

(Dextromethorphan HBr)

Relieves:

Cough up to 8 hours

For ages 12 & over

Alcohol 1.4%

Dosage Cup Included

Adult Tussin Cough Carton

Adult Tussin Cough Carton


ADULT TUSSIN COUGH 
dextromethorphan hydrobromide   liquid
Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)37808-300
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found
Product Characteristics
ColorREDScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#NDCPackage DescriptionMultilevel Packaging
137808-300-341 BOTTLE In 1 CARTONcontains a BOTTLE
1237 mL In 1 BOTTLEThis package is contained within the CARTON (37808-300-34)

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34105/05/1992

Labeler - H E B (007924756)
Revised: 07/2009H E B