Label: WALGREENS DAY AND NIGHT PACK- dextromethorphan hbr, guaifenesin, chlorpheniramine maleate kit
- NDC Code(s): 0363-7570-08, 0363-7571-04, 0363-7572-04
- Packager: WALGREEN CO
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 1, 2025
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- Children’s Daytime Wal-Tussin ®DM
- Active ingredients Day Time (in each 20 mL)
- Children’s Nighttime Wal-Tussin ®DM
- Active ingredients for Nighttime (in each 10 mL)
- Purposes for Daytime Wal-Tussin ®DM
- Purpose for Nighttime Wal-Tussin ®DM
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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
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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
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.
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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
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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
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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?
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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.
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INGREDIENTS AND APPEARANCE
WALGREENS DAY AND NIGHT PACK
dextromethorphan hbr, guaifenesin, chlorpheniramine maleate kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-7570 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-7570-08 1 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 Quantity Total Product Quantity Part 1 1 BOTTLE 118 mL Part 2 1 BOTTLE 118 mL Part 1 of 2 DAYTIME COUGH AND CHEST CONGESTION
dextromethorphan hbr, guaifenesin liquidProduct Information Item Code (Source) NDC:0363-7571 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 20 mg in 20 mL GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg in 20 mL Inactive Ingredients Ingredient Name Strength 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 Color purple Score Shape Size Flavor GRAPE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-7571-04 118 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 04/13/2020 Part 2 of 2 NIGHT TIME COUGH DM
chlorpheniramine maleate, diphenhydramine hbr liquidProduct Information Item Code (Source) NDC:0363-7572 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE 2 mg in 10 mL DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 15 mg in 10 mL Inactive Ingredients Ingredient Name Strength 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 Color red Score Shape Size Flavor FRUIT PUNCH Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-7572-04 118 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M010 04/13/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 04/13/2020 Labeler - WALGREEN CO (008965063)
