MUCINEX CHILDRENS FEVER SORE THROAT AND COUGH- acetaminophen, dextromethorphan hydrobromide solution 
RB Health (US) LLC

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Mucinex Children's Fever, Sore Throat & Cough

Drug Facts

Active ingredients / Purpose
(in each 10 mL)

Acetaminophen 325 mg..Pain reliever/fever reducer
Dextromethorphan HBr 10 mg....Cough suppressant

Acetaminophen 325 mg..Pain reliever/fever reducer
Dextromethorphan HBr 10 mg....Cough suppressant

Uses

■ temporarily relieves:
■ cough due to minor throat and bronchial irritation as
may occur with the common cold or inhaled irritants
■ the intensity of coughing
■ the impulse to cough to help your child get to sleep
■ minor aches and pains
■ sore throat
■ headache
■ temporarily reduces fever

Warnings
Liver warning: This product contains
acetaminophen. Severe liver damage may occur if
your child takes:
■ more than 5 doses in 24 hours, which is the
maximum daily amount
■ with other drugs containing acetaminophen
Allergy alert: Acetaminophen may cause severe
skin reactions. Symptoms may include:
■ skin reddening

■ blisters

■ rash


If a skin reaction occurs, stop use and seek medical help
right away.


Sore throat warning: If sore throat is severe, persists
for more than 2 days, is accompanied or followed by fever,
headache, rash, nausea, or vomiting, consult a doctor
promptly.

Do not use
■ with any other drug containing acetaminophen
(prescription or nonprescription). If you are not
sure whether a drug contains acetaminophen,
ask a doctor or pharmacist.
■ in a child who is 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 child’s prescription drug
contains an MAOI, ask a doctor or pharmacist
before giving this product.

Ask a doctor before use if the child has
■ liver disease
■ chronic cough that lasts such as occurs with
asthma
■ cough that occurs with too much phlegm
(mucus)

Ask a doctor or pharmacist before use if the child is
taking the blood thinning drug warfarin

Stop use and ask a doctor if
■ pain or cough gets worse or lasts more than
5 days
■ fever gets worse or lasts more than 3 days
■ redness or swelling is present
■ new symptoms occur
■ cough comes back or occurs with rash or
headache that lasts. These could be signs of a
serious condition.

Keep out of reach of children.


Overdose warning: Taking more than the recommended
dose (overdose) may cause liver damage. In case of
overdose, get medical help or contact a Poison Control
Center right away. Quick medical attention is critical even
if you do not notice any signs or symptoms

Directions

Directions
■ this product does not contain directions or complete
warnings for adult use
■ do not give more than directed (see Overdose
warning)
■ measure only with dosing cup provided
■ do not use dosing cup with other products
■ dose as follows or as directed by a doctor
■ children 6 to under 12 years of age: 10 mL in
dosing cup provided every 4 hours while
symptoms last; do not give more than 5 doses in
any 24-hour period
■ children under 6 years of age: do not use

Other information
■ each 10 mL contains: sodium 6 mg
■ store at 20-25°C (68-77°F)
■ do not refrigerate

Inactive ingredients: anhydrous citric acid,
D&C yellow no. 10, edetate disodium, FD&C red
no. 40, flavors, glycerin, propylene glycol,
purified water, sodium benzoate, sorbitol,
sucralose, xanthan gum

Questions? 1-866-682-4639

NDC 72854-064

Children's
Mucinex®

Honey
Flavor Liquid

4 FL OZ
(118 mL)

Label

MUCINEX CHILDRENS FEVER SORE THROAT AND COUGH 
acetaminophen, dextromethorphan hydrobromide solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72854-064
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg  in 10 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
XANTHAN GUM (UNII: TTV12P4NEE)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Product Characteristics
ColoryellowScore    
ShapeSize
FlavorHONEYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72854-064-041 in 1 CARTON05/01/2024
1118 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01205/01/2024
Labeler - RB Health (US) LLC (081049410)

Revised: 4/2024
Document Id: 1538a75d-582b-9501-e063-6394a90a6c55
Set id: 1538a75d-582a-9501-e063-6394a90a6c55
Version: 1
Effective Time: 20240403
 
RB Health (US) LLC