MAXIMUM STRENGTH MUCUS RELIEF DM- dextromethorphan hydrobromide and guaifenesin liquid 
Wal-Mart Stores,Inc.,

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Equate Maximum Strength Mucus Relief DM 6 FL OZ

Drug Facts

Active ingredients (in each 20 mL)Purposes

Dextromethorphan HBr 20 mg

Cough suppressant

Guaifenesin 400 mg

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 you 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 you have

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

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 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 right away at 1-800-222-2222.

Directions

do not take more than 6 doses in any 24-hour period
measure only with dosing cup provided
do not use dosing cup with other products
dose as follows or as directed by a doctor
mL = milliliter
adults and children 12 years and older: 20 mL every 4 hours
children under 12 years of age: Do not use

Other information

each 20 mL contains: sodium 8 mg
low sodium
store at room temperature
do not refrigerate
dosing cup provided

Inactive ingredients

anhydrous citric acid, edetate disodium, FD&C blue#1, FD&C red #40, natural and artificial flavor, potassium citrate , propylene glycol, propyl gallate, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum.

Questions or comments?

1-888-287-1915

PRINCIPAL DISPLAY PANEL

NDC# 49035-839-06

*Compare to the active ingredients in Maximum Strength Mucinex® Fast-MaxDM max

Maximum Strength

Mucus Relief DM

 
Dextromethorphan HBr Cough Suppressant
Guaifenesin Expectorant
 
Multi Symptom Relief
Chest Congestion
Cough
Thins & loosens Mucus
4 Hour Dosing
 
For Ages 12+

6 FL OZ (180 mL)

Tamper evident: do not use if printed seal under cap is broken or missing.

Maximum Strength per 4 hour dose.

DISTRIBUTED BY: Walmart Inc.,

Bentonville, AR 72716

*This product is not manufactured or distributed by Reckitt Benckiser, the owner of the registered trademark Maximum Strength Mucinex® Fast -Max® DM Max.

Equate Maximum Strength Mucus Relief DM 6FL OZ
MAXIMUM STRENGTH MUCUS RELIEF DM 
dextromethorphan hydrobromide and guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-839
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
dextromethorphan hydrobromide (UNII: 9D2RTI9KYH) (dextromethorphan - UNII:7355X3ROTS) dextromethorphan hydrobromide20 mg  in 20 mL
guaifenesin (UNII: 495W7451VQ) (guaifenesin - UNII:495W7451VQ) guaifenesin400 mg  in 20 mL
Inactive Ingredients
Ingredient NameStrength
anhydrous citric acid (UNII: XF417D3PSL)  
edetate disodium (UNII: 7FLD91C86K)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C red No. 40 (UNII: WZB9127XOA)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
propylene glycol (UNII: 6DC9Q167V3)  
propyl gallate (UNII: 8D4SNN7V92)  
water (UNII: 059QF0KO0R)  
sodium benzoate (UNII: OJ245FE5EU)  
sorbitol (UNII: 506T60A25R)  
sucralose (UNII: 96K6UQ3ZD4)  
xanthan gum (UNII: TTV12P4NEE)  
Product Characteristics
ColorREDScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-839-06180 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01205/01/2018
Labeler - Wal-Mart Stores,Inc., (051957769)

Revised: 12/2023
Document Id: 97bacb8f-c672-40cd-9f9d-f2aced8c7283
Set id: a748d5ab-901c-47bb-8437-997542ecebfe
Version: 6
Effective Time: 20231212
 
Wal-Mart Stores,Inc.,