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

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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

NIGHTTIME

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

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

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

Nighttime Wal-Tussin DM

Inactive ingredients

Inactive ingredients for Day TimeWal-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 TimeWal-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

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
Item Code (Source)NDC:0363-7571
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
1NDC:0363-7571-04118 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 DrugM01204/13/2020
Part 2 of 2
NIGHT TIME COUGH DM 
chlorpheniramine maleate, diphenhydramine hbr liquid
Product Information
Item Code (Source)NDC:0363-7572
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
1NDC:0363-7572-04118 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 DrugM01004/13/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01204/13/2020
Labeler - WALGREEN CO (008965063)

Revised: 12/2025
Document Id: 44e3b064-1d55-f8e8-e063-6294a90a3559
Set id: cb87e57b-ff06-4973-9751-137c7021e272
Version: 4
Effective Time: 20251201
 
WALGREEN CO