CHILDRENS MUCUS RELIEF CHERRY- dextromethorphan hydrobromide, guaifenesin liquid 
HEB

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredients

Dextromethorphan HBr, USP 5 mg
Guaifenesin, USP 100 mg

Purposes

Dextromethorphan HBr, USP...............Cough suppressant
Guaifenesin, USP...................................Expectorant

Uses

• helps loosen phlegm (mucus) and thin bronchial
secretions to rid the bronchial passageways of
bothersome mucus and make coughs more
productive
• 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

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 taking this product.

Ask a doctor before use if the child has

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

Stop use and ask a doctor if

• new symptoms occur
• redness or swelling is present
• fever gets worse or lasts more than 3 days
• pain or cough gets worse or lasts more than
5 days (children)
• cough comes back or occurs with fever, rash, or
headache that lasts. These could be signs
of a serious illness.

When using this product

• do not use more than directed

Keep this and all drugs out of the reach of children.

In case of accidental overdose, seek professional
assistance or contact a Poison Control Center
immediately.

Directions

• do not exceed 6 doses in a 24-hour period

age                                                                dose
children 6 years to under 12 years           1-2 teaspoonfuls (tsps)every 4 hours
children 4 years to under 6 years             1/2-1 teaspoonful (tsp)every 4 hours
children under 4 years                               do not use

Other Information

each teaspoon contains: sodium 3 mg
• store at controlled room temperature
• dosage cup provided

Inactive Ingredients

citric acid anhydrous,
dextrose, flavors, glycerin, methyl paraben, potassium
sorbate, propylene glycol, propyl paraben,
purified water, red 33, red 40, saccharin sodium,
sodium hydroxide, sucralose, xanthan gum

Principal Display Panel


image of label

CHILDRENS MUCUS RELIEF CHERRY 
dextromethorphan hydrobromide, guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59640-158
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE5 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
DEXTROSE (UNII: IY9XDZ35W2)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
SACCHARIN SODIUM ANHYDROUS (UNII: I4807BK602)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRY (Cherry Flavor) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59640-158-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/23/201006/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34103/23/201006/01/2017
Labeler - HEB (007924756)

Revised: 6/2017
 
HEB