Walgreen Co. Wal-Tussin® Drug Facts

Wal Tussin by

Drug Labeling and Warnings

Wal Tussin by is a Otc medication manufactured, distributed, or labeled by Walgreen Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WAL TUSSIN- dextromethorphan hydrobromide, guaifenesin liquid 
Walgreen Company

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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Walgreen Co. Wal-Tussin® Drug Facts

Active ingredient (in each 5 mL tsp)

Dextromethorphan HBr, USP 10 mg

Guaifenesin, USP 100 mg

Purpose

Cough suppressant

Expectorant

Uses

  • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
  • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

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, chronic bronchitis 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 6 doses in any 24-hour period
  • this adult product is not intended for use in children under 12 years of age

age

dose

adults and children

12 years and over

2 tsp every 4 hours

children under 12 years

do not use

Other information

  • store at 20°-25°C (68°-77°F)

Inactive ingredients

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

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to Robitussin® DM active ingredients

SEE NEW DOSING DIRECTIONS

Adult

WAL-TUSSIN®

COUGH AND CHEST CONGESTION

DM

Cough Suppressant (Dextromethorphan HBr)

Expectorant (Guaifenesin)

Relieves:

Coughs

Chest Congestion

Non-Drowsy

For Ages 12 & Over

Alcohol-Free

CHERRY FLAVOR

Wal-Tussin (R) Carton Image 1

Wal-Tussin® Carton Image 1

Wal-Tussin (R) Carton Image 2

Wal-Tussin® Carton Image 1

Wal-Tussin® Carton Image 2

WAL TUSSIN 
dextromethorphan hydrobromide, guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 0363-0359
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Product Characteristics
ColorRED (Orange-Red) Score    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 0363-0359-261 in 1 CARTON10/06/199505/14/2015
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC: 0363-0359-341 in 1 CARTON10/06/199504/12/2015
2237 mL in 1 BOTTLE; Type 0: Not a Combination Product
3NDC: 0363-0359-401 in 1 CARTON10/06/199505/20/2015
3355 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34110/06/199505/20/2015
Labeler - Walgreen Company (008965063)

Revised: 1/2020
Document Id: 575ab52d-139e-4e4e-8634-caa02b7611a2
Set id: 4412b49d-440f-46c6-8791-cc8f0819753c
Version: 3
Effective Time: 20200107
 
Walgreen Company