DAYTIME NIGHTTIME CHEWABLE- dextromethorphan hbr doxylamine succinate kit

Daytime Nighttime Chewable by

Drug Labeling and Warnings

Daytime Nighttime Chewable by is a Otc medication manufactured, distributed, or labeled by Walgreens. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each chewable gel) Daytime

Dextromethorphan HBr 10 mg 

Active ingredients for (in each chewable gel) NIGHTTIME

Dextromethorphan HBr 10 mg

Doxylamine Succinate 6.25 mg

Purpose for Daytime

Cough suppressant

Purposes for Nighttime

Cough suppressant

Antihistamine

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 

Warnings

Do not use

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

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

NIGHTTIME

taking sedatives or tranquilizers

When using this product

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

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,

DAYTIME NIGHTTIME

ask a health professional before use.

Keep out of reach of children.

DAYTIME / NIGHTTIME

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

Directions

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

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

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?

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

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

WALGREENS Childrens Daytime Nighttime Cough

INGREDIENTS AND APPEARANCE

DAYTIME NIGHTTIME CHEWABLE 
dextromethorphan hbr doxylamine succinate kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-9393

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-9393-32	1 in 1 KIT; Type 0: Not a Combination Product	04/30/2026

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 BOTTLE, PLASTIC	16
Part 2	1 BOTTLE, PLASTIC	16

Part 1 of 2

CHILDRENS DAYTIME MUCUS 
dextromethorphan hbr chewable gel

Product Information
Item Code (Source)	NDC: 0363-9358
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
WATER (UNII: 059QF0KO0R)
FD&C RED NO. 40 (UNII: WZB9127XOA)
MALIC ACID (UNII: 817L1N4CKP)
SUCROSE (UNII: C151H8M554)
SORBITOL (UNII: 506T60A25R)
GLYCERIN (UNII: PDC6A3C0OX)
SUCRALOSE (UNII: 96K6UQ3ZD4)
GLYCYRRHIZIN (UNII: 6FO62043WK)
CORN SYRUP (UNII: 9G5L16BK6N)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
PECTIN (UNII: 89NA02M4RX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
ALCOHOL (UNII: 3K9958V90M)
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)

Product Characteristics
Color	red	Score	no score
Shape	ROUND	Size
Flavor	BERRY (Mixed Berry)	Imprint Code	7
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-9358-16	16 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	04/30/2026

Part 2 of 2

CHILDRENS NIGHTTIME MUCUS 
dextromethorphan hbr doxylamine succinate chewable gel

Product Information
Item Code (Source)	NDC: 0363-9360
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg
DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL)	DOXYLAMINE SUCCINATE	6.25 mg

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
CORN SYRUP (UNII: 9G5L16BK6N)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
SUCRALOSE (UNII: 96K6UQ3ZD4)
GLYCERIN (UNII: PDC6A3C0OX)
SUCROSE (UNII: C151H8M554)
GLYCYRRHIZIN (UNII: 6FO62043WK)
MALIC ACID (UNII: 817L1N4CKP)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
PECTIN (UNII: 89NA02M4RX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)

Product Characteristics
Color	purple	Score	no score
Shape	ROUND	Size
Flavor	BERRY (Mixed Berry)	Imprint Code	P
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-9360-16	16 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	04/30/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	04/30/2026

Labeler - Walgreens (008965063)