FDA.reportPublic FDA data

Drug Facts

Manufacturer
Walgreens
Effective date
2026-04-15
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:55:26

Label at a glance#

ProductDaytime Nighttime Chewable
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
Label structure12 sections

Indications and uses

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

Dosage and administration

DAYTIME / NIGHTTIME take every 4 hours or as directed by a doctor chew thoroughly before swallowing adults and children 12 years of age and over: 2 chewable gels every 4 hours, not to exceed 12 chewable gels in any 24-hour period children 6 to under 12 years of age: 1 chewable gel every 4 hours, not to exceed 6 chewable gels in any 24-hour period children under 6 years of age: do not use 

Storage and handling

DAYTIME each chewable gel contains: sodium 8 mg store between 20-25ºC (68-77º). Do not refrigerate NIGHTTIME each chewable gel contains sodium 6 mg store between 20-25ºC (68-77ºF). Do not refrigerate

Label contents#

Full prescribing information#

Active ingredient (in each chewable gel) Daytime

OTC - ACTIVE INGREDIENT SECTION

Dextromethorphan HBr 10 mg 

Active ingredients for (in each chewable gel) NIGHTTIME

OTC - ACTIVE INGREDIENT SECTION

Dextromethorphan HBr 10 mg

Doxylamine Succinate 6.25 mg

Purpose for Daytime

OTC - PURPOSE SECTION

Cough suppressant

Purposes for Nighttime

OTC - PURPOSE SECTION

Cough suppressant

Antihistamine

Uses

INDICATIONS & USAGE SECTION

DAYTIME

  • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold

NIGHTTIME

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

Warnings

WARNINGS SECTION

Do not use

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 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)
  • persistent or chronic cough such as occurs with smoking, asthma or emphysema

NIGHTTIME

  • glaucoma
  • 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
  • trouble urinating due to enlarged prostate gland

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

DAYTIME

do not use more than directed.

NIGHTTIME

  • do not exceed recommended dosage
  • excitability may occur, especially in children
  • marked drowsiness may occur
  • avoid alcoholic drinks
  • alcohol, sedatives and tranquilizers may increase drowsiness
  • use caution when driving a motor vehicle or operating machinery 

Stop use and ask a doctor if

OTC - STOP USE SECTION

DAYTIME 

cough lasts more than 7 days, comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition.

NIGHTTIME

cough lasts 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 NIGHTTIME

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

DAYTIME / 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 / NIGHTTIME

  • take every 4 hours or as directed by a doctor
  • chew thoroughly before swallowing
  • adults and children 12 years of age and over: 2 chewable gels every 4 hours, not to exceed 12 chewable gels in any 24-hour period
  • children 6 to under 12 years of age: 1 chewable gel every 4 hours, not to exceed 6 chewable gels in any 24-hour period
  • children under 6 years of age: do not use 

Other information

STORAGE AND HANDLING SECTION

DAYTIME

  • each chewable gel contains: sodium 8 mg
  • store between 20-25ºC (68-77º). Do not refrigerate

NIGHTTIME

  • each chewable gel contains sodium 6 mg
  • store between 20-25ºC (68-77ºF). Do not refrigerate

Inactive ingredient

INACTIVE INGREDIENT SECTION

DAYTIME 

ammonium glycyrrhizate, anhydrous citric acid, corn syrup, FD&C red # 40, flavors, glycerin, glycyrrhizin, malic acid, maltodextrin, medium-chain triglycerides, pectin, propylene glycol, purified water, sorbitol solution, sucralose, sucrose, trisodium citrate dihydrate 

NIGHTTIME 

alcohol, ammonium glycyrrhizate, anhydrous citric acid, corn syrup, FD&C blue #1, FD&C Red #40, flavors, glycerin, glycyrrhizin, malic acid, maltodextrin, pectin, propylene glycol, purified water, sucralose, sucrose, trisodium citrate dihydrate 

Questions or comments?

OTC - QUESTIONS SECTION

Call1-877-753-3935 Monday-Friday 9AM-5PM EST 

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to the active ingredients in Children's Mucinex® Daytime Mighty Chews & Children's Mucinex® Nighttime Mighty Chews††

Children's Cough

DEXTROMETHORPHAN HBr 10 mg /

COUGH SUPPRESSANT

Daytime

  • Controls cough
  • Up to 4-hours of relief

AGES 6+ YEARS 

SOLID CHEWABLE GELS  

Mixed Berry flavor

††This product is not manufactured or distributed by RB Health (US) LLC, distributor of Mucinex® Children's Mighty Chews Cough Daytime.

NightTime

Children's 

Cough

DEXTROMETHORPHAN HBr 10 mg /

COUGH SUPPRESSANT

DOXYLAMINE SUCCINATE 6.25 mg /

ANTHIHISTAMINE

Nighttime

  • Controls cough to help you get to sleep

AGES 6+ YEARS

SOLID CHEWABLE GELS

Mixed Berry flavor

††This product is not manufactured or distributed by RB Health (US) LLC, distributor of Mucinex® Children's Mighty Chews Cough Nighttime

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

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT UNFORMATION

DISTRIBUTED BY WALGREEN CO.

DEEREFIELD, IL 60015

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WALGREENS Childrens Daytime Nighttime Cough
WALGREENS Childrens Daytime Nighttime Cough

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2683425{1 (dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG Chewable Tablet) / 1 (dextromethorphan hydrobromide 10 MG Chewable Tablet) } PackGPCK8
26834251 daytime (dextromethorphan HBr 10 MG Chewable Tablet) / 1 nighttime (dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG Chewable Tablet) PackPSN8
2683423dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG Chewable TabletPSN8
2683424dextromethorphan hydrobromide 10 MG Chewable TabletPSN8
2683423dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG Chewable TabletSCD8
2683424dextromethorphan hydrobromide 10 MG Chewable TabletSCD8
26834251 daytime (dextromethorphan HBr 10 MG Chewable Tablet) / 1 nighttime (dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG Chewable Tablet) PackSY8
2683423dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG Chewable TabletSY8
2683424dextromethorphan HBr 10 MG Chewable TabletSY8

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DEXTROMETHORPHAN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
DOXYLAMINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
59361619-24d9-b610-eca6-5a7f25ed5e03Product name520240909
f4368033-af8c-41bf-a84b-ff77392b8522Product name120161229

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-9358-16Daytime Nighttime Chewable16 in 1 BOTTLE, PLASTICCHEWABLE GEL1610 mg8
0363-9360-16Daytime Nighttime Chewable16 in 1 BOTTLE, PLASTICCHEWABLE GEL166.25 mg8
0363-9393-32Daytime Nighttime Chewable1 in 1 KITKIT18

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-93930363-9393-32
0363-93580363-9358-16
0363-93600363-9360-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 matching rows.

Name, UNII, Kind table
NameUNIIKind
DEXTROMETHORPHAN HYDROBROMIDE9D2RTI9KYHACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
WATER059QF0KO0RIACT
FD&C RED NO. 40WZB9127XOAIACT
MALIC ACID817L1N4CKPIACT
SUCROSEC151H8M554IACT
SORBITOL506T60A25RIACT
GLYCERINPDC6A3C0OXIACT
SUCRALOSE96K6UQ3ZD4IACT
GLYCYRRHIZIN6FO62043WKIACT
CORN SYRUP9G5L16BK6NIACT
MALTODEXTRIN7CVR7L4A2DIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
PECTIN89NA02M4RXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
TRISODIUM CITRATE DIHYDRATEB22547B95KIACT
ALCOHOL3K9958V90MIACT
AMMONIUM GLYCYRRHIZATE3VRD35U26CIACT
DEXTROMETHORPHAN HYDROBROMIDE9D2RTI9KYHACTIB
DOXYLAMINE SUCCINATEV9BI9B5YI2ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
FD&C RED NO. 40WZB9127XOAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
CORN SYRUP9G5L16BK6NIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
AMMONIUM GLYCYRRHIZATE3VRD35U26CIACT
SUCRALOSE96K6UQ3ZD4IACT
GLYCERINPDC6A3C0OXIACT
SUCROSEC151H8M554IACT
GLYCYRRHIZIN6FO62043WKIACT
MALIC ACID817L1N4CKPIACT
MALTODEXTRIN7CVR7L4A2DIACT
PECTIN89NA02M4RXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
TRISODIUM CITRATE DIHYDRATEB22547B95KIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42026-02-13monthly-update2026-06-03 17:58:09

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 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Childrens Daytime MucusDEXTROMETHORPHAN HBRWalgreens7a55b7e1-1054-421e-847e-5e4d90d1aebb2026-04-15WarningsExact identifier
ndc (package): 0363-9358-16
ndc (product): 0363-9358
ndc11 (package): 00363935816
Childrens Nighttime MucusDEXTROMETHORPHAN HBR DOXYLAMINE SUCCINATEWalgreensdc69f581-27c7-4030-bb18-39685c7691a12026-04-15WarningsExact identifier
ndc (package): 0363-9360-16
ndc (product): 0363-9360
ndc11 (package): 00363936016
Daytime Nighttime ChewableDEXTROMETHORPHAN HBR DOXYLAMINE SUCCINATEWalgreens9ddc0aa7-e7b8-41c5-a2b4-fece0c2e26c62026-04-15WarningsExact identifier
ndc (package): 0363-9358-16
ndc (package): 0363-9360-16
ndc (package): 0363-9393-32
ndc (product): 0363-9393
ndc11 (package): 00363939332
ndc11 (package): 00363935816
ndc11 (package): 00363936016
spl id: e0973deb-d8ac-4180-9bc5-bbf6ec75cc57
spl set id: 9ddc0aa7-e7b8-41c5-a2b4-fece0c2e26c6

Reported adverse events (FAERS/openFDA)#

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