CHILDRENS DAYTIME MUCUS- dextromethorphan hbr chewable gel

Childrens Daytime Mucus by

Drug Labeling and Warnings

Childrens Daytime Mucus 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)

Dextromethorphan HBr 10 mg

Purpose

Cough suppressant

Use

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

Warnings

Do not use

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 giving this product.

Ask a doctor before use if you have

• cough that occurs with too much phlegm (mucus)
• persistent or chronic cough such as occurs with smoking, asthma, emphysema

When using this product

do not use more than directed.

Stop use and ask a doctor if

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.

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 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

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

Inactive ingredients

ammonium glycyrrhizate, anhydrous citric acid, corn syrup, FD&C Red No. 40, flavors, glycerin, glycyrrhizin, malic acid, maltodextrin, medium-chain triglycerides, pectin, propylene glycol, purified water, sorbitol solution, 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

Daytime

• Controls cough
• Up to 4-hours of relief

AGES 6+ YEARS

SOLID CHEWABLE GELS

Mixed Berry Flavor

FL OZ (mL)

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

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 Mixed Berry Flavor

INGREDIENTS AND APPEARANCE

CHILDRENS DAYTIME MUCUS 
dextromethorphan hbr chewable gel

Product Information
Product Type	HUMAN OTC DRUG	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)
WATER (UNII: 059QF0KO0R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
MALIC ACID (UNII: 817L1N4CKP)
CORN SYRUP (UNII: 9G5L16BK6N)
FD&C RED NO. 40 (UNII: WZB9127XOA)
SUCROSE (UNII: C151H8M554)
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCYRRHIZIN (UNII: 6FO62043WK)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
PECTIN (UNII: 89NA02M4RX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SORBITOL SOLUTION (UNII: 8KW3E207O2)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)

Product Characteristics
Color	red	Score	no score
Shape	ROUND (Gumdrop)	Size
Flavor	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	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)