Walgreens Childrens

Manufacturer: WALGREENS CO.
Effective date: 2025-12-01
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-06-01 01:18:55

Label at a glance#

ProductWalgreens Childrens

Active ingredientCHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE

Label structure9 sections

Indications and uses

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

Dosage and administration

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

Storage and handling

each 10 mL contains: sodium 3 mg store at room temperature. Do not refrigerate contain low sodium do not use if printed seal under cap is torn or missing

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact1-866-467-2748

Label contents#

Full prescribing information#

Active ingredients (in each 10 mL)

OTC - ACTIVE INGREDIENT SECTION

Chlorpheniramine maleate, USP 2 mg

Dextromethorphan HBr USP 15 mg

Purpose

OTC - PURPOSE SECTION

Antihistamine

Cough suppressant

Uses

INDICATIONS & USAGE SECTION

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

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

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

taking sedatives or tranquilizers.

When using this product

OTC - WHEN USING SECTION

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

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

ask a health professional before use

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

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

each 10 mL contains: sodium 3 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

anhydrous citric acid, FD&C Red # 40, flavor, potassium sorbate, potassium citrate, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose

Questions or comments?

OTC - QUESTIONS SECTION

1-866-467-2748

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to the Children's Robitussin ^®Nighttime Cough DM active ingredients ^††

NDC# 0363-7560-04

Children's

Nighttime Cough

Wal-Tussin ^®DM

CHLORPHENIRAMINE MALEATE, USP 2 mg/10 mL

ANTIHISTAMINE

DEXTROMETHORPHAN HBr, USP 15 mg/15 mL

COUGH SUPPRESSANT

NIGHTTIME

Relieves cough & runny nose

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)

Walgreens PHARMACIST RECOMMENDED ^†

Health expertise you rely on, quality you trust

^†Walgreens Pharmacists Survey

^*This product is not manufactured or distributed by Pfizer, owner of the registered trademarks Children’s Robitussin ^®

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

Walgreens

100% SATISFACTION GUARANTEED

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1111440	Chlorpheniramine/Dextromethorphan (Oral Liquid)	chlorpheniramine maleate 0.2 MG/ML / dextromethorphan hydrobromide 1.5 MG/ML Oral Solution	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1111440	chlorpheniramine maleate 1 MG / dextromethorphan HBr 7.5 MG in 5 mL Oral Solution	PSN	7
1111440	chlorpheniramine maleate 0.2 MG/ML / dextromethorphan hydrobromide 1.5 MG/ML Oral Solution	SCD	7
1111440	chlorpheniramine maleate 1 MG / dextromethorphan hydrobromide 7.5 MG per 5 ML Oral Solution	SY	7
1111440	chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 15 MG per 10 ML Oral Solution	SY	7

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
CHLORPHENIRAMINE Pharmacologic Class Indexing	3	Indexing - Pharmacologic Class	20180813
DEXTROMETHORPHAN Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d17a97fa-387f-690e-d2be-0083ab044a03	Product name	3	20170725
0fdb98e2-b951-a1ce-5715-2b187ba500ef	Product name	4	20170718
c6fba691-a132-4ede-95c6-f8c6bd696636	Product name	1	20150902
c0200ab5-4954-454e-9676-30b741b245bd	Product name	1	20150730

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0363-7560-04	2023-01-30	C162847	48780-1	f386c64a-3720-0266-e053-dadaa90a7c1a	Walgreens Children’s Night-Time Cough & Chest Congestion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0363-7560-04	Walgreens Childrens	118 mL in 1 BOTTLE	LIQUID	118		7

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

Walgreens Childrens
Nighttime Cough
ANHYDROUS CITRIC ACID
FD&C RED NO. 40
GLYCERIN
LACTIC ACID, UNSPECIFIED FORM
POTASSIUM SORBATE
PROPYLENE GLYCOL
WATER
SODIUM BENZOATE
SODIUM CITRATE, UNSPECIFIED FORM
SORBITOL
SUCRALOSE
CHLORPHENIRAMINE MALEATE
CHLORPHENIRAMINE
DEXTROMETHORPHAN HYDROBROMIDE
DEXTROMETHORPHAN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0363-7560	0363-7560-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
GLYCERIN	PDC6A3C0OX	IACT
LACTIC ACID, UNSPECIFIED FORM	33X04XA5AT	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
SODIUM CITRATE, UNSPECIFIED FORM	1Q73Q2JULR	IACT
SORBITOL	506T60A25R	IACT
SUCRALOSE	96K6UQ3ZD4	IACT
CHLORPHENIRAMINE MALEATE	V1Q0O9OJ9Z	ACTIB
DEXTROMETHORPHAN HYDROBROMIDE	9D2RTI9KYH	ACTIB

Source Document#

Source XML

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Walgreens Childrens	NIGHTTIME COUGH	WALGREENS CO.	a270cbe3-bf0a-44da-9359-00e218eba239	2025-12-01	Warnings	Exact identifier ndc (package): 0363-7560-04 ndc (product): 0363-7560 ndc11 (package): 00363756004 spl id: 44e1c78e-5a2e-a020-e063-6394a90ab73a spl set id: a270cbe3-bf0a-44da-9359-00e218eba239

Reported adverse events (FAERS/openFDA)#

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