CHILDRENS NIGHTTIME MUCUS- dextromethorphan hbr doxylamine succinate chewable gel

Childrens Nighttime Mucus by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredients (in each chewable gel)

Dextromethorphan HBr 10 mg

Doxylamine Succinate 6.25 mg 

Purposes

Cough suppressant

Antihistamine

Uses

• 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
  • sneezing
  • itching of the nose or throat
  • itchy, water eyes

Warnings

Do not use

• 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 the child has

• glaucoma
• cough that occurs with too much phlegm (mucus)
• a breathing problem or chronic cough that lasts or 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

taking sedatives or tranquilizers

When using this product

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

Stop use and ask a doctor if

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,

ask a health professional before use

Keep out of reach of children.

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

Directions

• take every 4 hours, or as directed by a doctor
• chew thoroughly before swallowing
• adults and children 12 years 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

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

Inactive ingredients

alcohol, ammonium glycyrrhizate, anhydrous citric acid, corn syrup, FD&C Blue No 1, FD&C Red No 40, flavors, glycerin, glycyrrhizin, malic acid, maltodextrin, pectin, propylene glycol, purified water, sucralose, sucrose, trisodium citrate dihydrate

Questions or comments?

Call 1-877-753-3929 Monday-Friday 9AM-5PM EST

Principal Display Panel

Children's Cough

DEXTROMETHORPHAN HBr 10 mg

COUGH SUPPRESSANT

DOXYLAMINE SUCCINATE 6.25 mg 

ANTIHISTAMINE

Nighttime

• Controls cough to help you get to sleep

AGES 6+ YEARS

SOLID CHEWABLE GELS

Mixed Berry flavor

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

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

DISTRIBUTED BY: WALGREEN CO.

DEERFIELD, IL 60015

Package Label

WALGREENS Children's Cough Chewable Gel Mixed berry flavor

INGREDIENTS AND APPEARANCE

CHILDRENS NIGHTTIME MUCUS 
dextromethorphan hbr doxylamine succinate chewable gel

Product Information
Product Type	HUMAN OTC DRUG	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)
CORN SYRUP (UNII: 9G5L16BK6N)
WATER (UNII: 059QF0KO0R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SUCROSE (UNII: C151H8M554)
FD&C RED NO. 40 (UNII: WZB9127XOA)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
ALCOHOL (UNII: 3K9958V90M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCYRRHIZIN (UNII: 6FO62043WK)
MALIC ACID (UNII: 817L1N4CKP)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
PECTIN (UNII: 89NA02M4RX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Product Characteristics
Color	purple	Score	no score
Shape	ROUND (Gumdrop)	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	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)