WALGREENS DAY AND NIGHT PACK- dextromethorphan hbr, guaifenesin, chlorpheniramine maleate 
WALGREEN CO

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 Children’s Daytime & Night-Time Cough and Chest Congestion DM

Children’s Daytime Wal-Tussin® DM

Active ingredients Day Time (in each 20 mL)

Dextromethorphan HBr USP 20 mg

Guaifenesin. USP 200 mg

Children’s Nighttime Wal-Tussin® DM

Active ingredients for Nighttime (in each 10 mL)

Chlorpheniramine maleate, USP 2 mg

Dextromethorphan HBr USP 15 mg

Purposes for Daytime Wal-Tussin® DM

Cough suppressant

Expectorant

Purpose for Nighttime Wal-Tussin® DM

Antihistamine

Cough suppressant

Uses

DAYTIME

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

NIGHTTIME

temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
runny nose
sneezing
itching of the nose or throat 
itchy, watery eyes

Warnings

Do not us

DAYTIME

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.

NIGHTTIME

to sedate a child or to make a child sleepy
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

DAYTIME

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

NIGHTTIME

trouble urinating due to an enlarges prostate gland
glaucoma
a cough that occurs with too much phlegm (mucus)
a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis or emphysema

Ask a doctor or pharmacist before use if you are

NIGHTTIME

taking sedatives or tranquilizers.

When using this product

NIGHTTIME

do not use more than directed.
marked drowsiness may occur
avoid alcoholic drinks
alcohol, sedatives and tranquilizers may increase drowsiness
be careful when driving a motor vehicle or operating machinery
excitability may occur, especially in children

Stop use and ask a doctor if

DAYTIME

cough last more than 7 days, comes back or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

NIGHTTIME

cough last 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,

DAYTIME

ask a health professional before use.

NIGHTTIME

ask a health professional before use

Keep out of reach of children.

DAYTIME

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

NIGHTTIME

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away

Directions

Daytime Wal-Tussin® DM

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

age

dose

Children under 4 years

Do not use

Children 4 to under 6 years

5 mL every 4 hours

Children 6 to under 12 years

10 mL every 4 hours

Adults and children 12 years and older

20 mL every 4 hours


Nighttime Wal-Tussin® DM

do not take more than 4 doses in any 24-hour period
measure only with dosing cup provided.
keep dosing cup with product
mL= milliliter

age

dose

Children under 6 years

Do not use

Children 6 to under 12 years

10 mL every 6 hours

Adults and children 12 years and older

20 mL every 6 hours

Other information

DAYTIME Wal-Tussin DM

each 20 mL contains: sodium 11 mg
store at room temperature. Do not refrigerate
contain low sodium
do not use if printed seal under cap is torn or missing

Nighttime Wal-Tussin DM

each 10 mL contains: sodium 6 mg
store at room temperature. Do not refrigerate
contain low sodium
do not use if printed seal under cap is torn or missing

Inactive ingredients

Inactive ingredients for Day Time Wal-Tussin DM 

anhydrous citric acid, carboxymethylcellulose sodium, edetate disodium, FD &C Blue No. 1, FD&C Red No. 40, natural and artificial flavors, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum

Inactive ingredients for Night Time Wal-Tussin DM 

anhydrous citric acid, FD&C Red No. 40, natural and artificial flavors, glycerin, lactic acid, potassium sorbate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose

Questions or comments?

1-866-467-2748

Principal Display Panel

Compare to Children's Robitussin® Cough & Chest Congestion DM* & Nighttime Cough DM Long-Active active ingredients††

Children's

Cough & Chest Congestions DM

Wal-Tussin® DM

DEXTROMETHORPHAN HBr, USP 20 mg/ 20 mL

COUGH SUPPRESSANT

GUAIFENESIN, USP 200 mg

EXPECTORANT

DAYTIME

NON-DROWSY

Relieves cough, chest congestion & mucus

4 YEARS & OVER

GRAPE FLAVOR

Naturally and Artificially Flavored

Dosage cup included

2 - 4 FL OZ (118 mL) BOTTLES / TOTAL – 8 FL OZ (236 mL)

††This product is not manufactured or distributed by Pfizer, the distributor of Children’s Robitussin® Cough & Chest Congestion DM.

Children's

Nighttime Cough DM

Wal-Tussin® DM

CHLORPHENIRAMINE MALEATE, USP 2 mg / 10 mL

ANTIHISTAMINE

DEXTROMETHORPHAN HBr, USP 15 mg / 10 mL

COUGH SUPPRESSANT

NIGHTTIME

Relieves cough & runny nose

Alcohol free

6 YEARS & OLDER

Fruit Punch Flavor

Naturally and Artificially Flavored

Dosage cup included

2 - 4 FL OZ (118 mL) BOTTLES TOTAL – 8 FL OZ (236 mL)

††This product is not manufactured or distributed by Pfizer, the distributor of Children’s Robitussin® Nighttime Cough DM Long-Acting.

Walgreens

PHARMACIST RECOMMENDED

TAMPER EVIDENT: DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS BROKEN OR MISSING

DISTRIBUTED BY: WALGREENS CO.

200 WILMOT RD. DEERFIELD, IL 60015

Walgreens 10% SATISFACTION GUARANTEED

walgreens.com ©2020 Walgreen Co.

Walgreens Childrens Day Time & Nighttime Wal Tussin DM Twin Pack
WALGREENS DAY AND NIGHT PACK 
dextromethorphan hbr, guaifenesin, chlorpheniramine maleate kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-7570
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-7570-081 in 1 KIT; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)04/13/2020
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE 118 mL
Part 21 BOTTLE 118 mL
Part 1 of 2
DAYTIME COUGH AND CHEST CONGESTION 
dextromethorphan hbr, guaifenesin liquid
Product Information
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg  in 20 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorPURPLEScore    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1118 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34104/13/2020
Part 2 of 2
NIGHT TIME COUGH DM 
chlorpheniramine maleate, diphenhydramine hbr liquid
Product Information
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE2 mg  in 10 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Product Characteristics
ColorREDScore    
ShapeSize
FlavorFRUIT PUNCHImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1118 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34104/13/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34104/13/2020
Labeler - WALGREEN CO (008965063)

Revised: 1/2022
Document Id: 5690c1c4-3812-455d-9b72-be9185479c9c
Set id: cb87e57b-ff06-4973-9751-137c7021e272
Version: 2
Effective Time: 20220112
 
WALGREEN CO