FDA.reportPublic FDA data

Walgreens DAY and NIGHT PACK

Manufacturer
WALGREEN CO
Effective date
2025-12-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:18:58

Label at a glance#

ProductWalgreens DAY and NIGHT PACK
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, CHLORPHENIRAMINE MALEATE
Label structure11 sections

Indications and 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 ...

Dosage and administration

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 a...

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredients Day Time (in each 20 mL)

OTC - ACTIVE INGREDIENT SECTION

Dextromethorphan HBr USP 20 mg

Guaifenesin. USP 200 mg

Active ingredients for Nighttime (in each 10 mL)

OTC - ACTIVE INGREDIENT SECTION

Chlorpheniramine maleate, USP 2 mg

Dextromethorphan HBr USP 15 mg

Purposes for Daytime Wal-Tussin ®DM

OTC - PURPOSE SECTION

Cough suppressant

Expectorant

Purpose for Nighttime Wal-Tussin ®DM

OTC - PURPOSE SECTION

Antihistamine

Cough suppressant

Uses

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Do not us

OTC - DO NOT USE SECTION

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

OTC - ASK DOCTOR SECTION

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

OTC - ASK DOCTOR/PHARMACIST SECTION

NIGHTTIME

taking sedatives or tranquilizers.

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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,

OTC - PREGNANCY OR BREAST FEEDING SECTION

DAYTIME

ask a health professional before use.

NIGHTTIME

ask a health professional before use

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

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 INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

1-866-467-2748

Principal Display Panel

PACKAGE LABEL.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 Childrens Day Time & Nighttime Wal Tussin DM Twin Pack

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2362250{1 (chlorpheniramine maleate 0.2 MG/ML / dextromethorphan hydrobromide 1.5 MG/ML Oral Solution) / 1 (dextromethorphan hydrobromide 1 MG/ML / guaifenesin 10 MG/ML Oral Solution) } PackGPCK4
23622501 daytime (dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 20 mL Oral Solution) / 1 nighttime (chlorpheniramine maleate 2 MG / dextromethorphan HBr 15 MG in 10 mL Oral Solution) PackPSN4
1111440chlorpheniramine maleate 1 MG / dextromethorphan HBr 7.5 MG in 5 mL Oral SolutionPSN4
1790650dextromethorphan HBr 10 MG / guaiFENesin 100 MG in 10 mL Oral SolutionPSN4
1111440chlorpheniramine maleate 0.2 MG/ML / dextromethorphan hydrobromide 1.5 MG/ML Oral SolutionSCD4
1790650dextromethorphan hydrobromide 1 MG/ML / guaifenesin 10 MG/ML Oral SolutionSCD4
23622501 daytime (dextromethorphan HBr 20 MG / guaifenesin 200 MG per 20 ML Oral Solution) / 1 nighttime (chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 15 MG per 10 ML Oral Solution) PackSY4
1111440chlorpheniramine maleate 1 MG / dextromethorphan hydrobromide 7.5 MG per 5 ML Oral SolutionSY4
1111440chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 15 MG per 10 ML Oral SolutionSY4
1790650dextromethorphan HBr 10 MG / guaifenesin 100 MG per 10 ML Oral SolutionSY4
1790650dextromethorphan HBr 20 MG / guaifenesin 200 MG per 20 ML Oral SolutionSY4
1790650dextromethorphan HBr 5 MG / guaifenesin 50 MG per 5 ML Oral SolutionSY4

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CHLORPHENIRAMINE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813
DEXTROMETHORPHAN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
GUAIFENESIN Pharmacologic Class Indexing1Indexing - Pharmacologic Class20211129

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130311917177007GTIN-13: 0311917177007
EAN-13: 0311917177007
GTIN-12: 311917177007
UPC-A: 311917177007
GTIN storage (14 digits): 00311917177007		image-01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d17a97fa-387f-690e-d2be-0083ab044a03Product name320170725
0fdb98e2-b951-a1ce-5715-2b187ba500efProduct name420170718
c6fba691-a132-4ede-95c6-f8c6bd696636Product name120150902
c0200ab5-4954-454e-9676-30b741b245bdProduct name120150730
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0363-7570-082024-11-25C16284748780-11030e365-1ed0-111a-e063-dadaa90a10e2Walgreen Children’s Daytime & Night-Time Cough and Chest Congestion DM
0363-7570-082024-01-30C16284748780-11030e365-1ed0-111a-e063-dadaa90a10e2Walgreen Children’s Daytime & Night-Time Cough and Chest Congestion DM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-7570-08Walgreens DAY and NIGHT PACK1 in 1 KITKIT14
0363-7571-04Walgreens DAY and NIGHT PACK118 mL in 1 BOTTLELIQUID118 mL200 mg in 20mL4
0363-7572-04Walgreens DAY and NIGHT PACK118 mL in 1 BOTTLELIQUID118 mL2 mg in 10mL4

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-75700363-7570-08
0363-75710363-7571-04
0363-75720363-7572-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIEDK679OBS311IACT
EDETATE DISODIUM7FLD91C86KIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C RED NO. 40WZB9127XOAIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM CITRATE, UNSPECIFIED FORM1Q73Q2JULRIACT
SORBITOL506T60A25RIACT
SUCRALOSE96K6UQ3ZD4IACT
XANTHAN GUMTTV12P4NEEIACT
DEXTROMETHORPHAN HYDROBROMIDE9D2RTI9KYHACTIB
GUAIFENESIN495W7451VQACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
FD&C RED NO. 40WZB9127XOAIACT
GLYCERINPDC6A3C0OXIACT
LACTIC ACID, UNSPECIFIED FORM33X04XA5ATIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
SODIUM BENZOATEOJ245FE5EUIACT
SODIUM CITRATE, UNSPECIFIED FORM1Q73Q2JULRIACT
SORBITOL506T60A25RIACT
SUCRALOSE96K6UQ3ZD4IACT
CHLORPHENIRAMINE MALEATEV1Q0O9OJ9ZACTIB
DEXTROMETHORPHAN HYDROBROMIDE9D2RTI9KYHACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Walgreens DAY and NIGHT PACKDEXTROMETHORPHAN HBR, GUAIFENESIN, CHLORPHENIRAMINE MALEATEWALGREEN COcb87e57b-ff06-4973-9751-137c7021e2722025-12-01WarningsExact identifier
ndc (package): 0363-7572-04
ndc (package): 0363-7570-08
ndc (package): 0363-7571-04
ndc (product): 0363-7570
ndc11 (package): 00363757008
ndc11 (package): 00363757104
ndc11 (package): 00363757204
spl id: 44e3b064-1d55-f8e8-e063-6294a90a3559
spl set id: cb87e57b-ff06-4973-9751-137c7021e272

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.