Label: MAXIMUM STRENGTH MUCUS RELIEF SEVERE CONGESTION AND COUGH- dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride liquid
- NDC Code(s): 49035-774-06
- Packager: Wal-Mart Stores,Inc.,
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2024
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
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Uses
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- helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
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- temporarily relieves:
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- cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants
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- the intensity of coughing
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- the impulse to cough to help you get to sleep
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- nasal congestion due to a cold
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Warnings
Do not use
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- 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
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- heart disease
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- high blood pressure
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- thyroid disease
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- diabetes
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- trouble urinating due to an enlarged prostate gland
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- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema
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- cough that occurs with too much phlegm (mucus)
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Directions
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- do not take more than 6 doses in any 24-hour period
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- measure only with dosing cup provided
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- do not use dosing cup with other products
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- dose as follows or as directed by a doctor
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- mL = milliliter
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- Adults and children 12 years of age and older: 20 mL in dosing cup provided every 4 hours.
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- Children under 12 years of age: Do not use.
- Other information
- Inactive ingredients
- Questions or comments?
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PRINCIPAL DISPLAY PANEL
NDC 49035-774-06
Compare to Mucinex® Fast- Max® Maximum Strength Severe Congestion & Cough Active Ingredients*
Maximum Strength‡
Severe Congestion & Cough
Dextromethorphan HBr - Cough Suppressant
Guaifenesin - Expectorant
Phenylephrine HCl - Nasal DecongestantMAXIMUM STRENGTH
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- Controls cough
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- Relieves nasal and chest congestion
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- Thins & loosens mucus
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
Satisfaction guaranteed – Or we will replace it or give you your money back. For questions or comments or to report an undesired reaction or side effect, please call 1-888-287-1915.
*This product is not manufactured or distributed by Reckitt Benckiser, the owner of the registered trademark Mucinex® Fast -Max® Maximum Strength Severe Congestion & Cough.
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INGREDIENTS AND APPEARANCE
MAXIMUM STRENGTH MUCUS RELIEF SEVERE CONGESTION AND COUGH
dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-774 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength dextromethorphan hydrobromide (UNII: 9D2RTI9KYH) (dextromethorphan - UNII:7355X3ROTS) dextromethorphan hydrobromide 20 mg in 20 mL guaifenesin (UNII: 495W7451VQ) (guaifenesin - UNII:495W7451VQ) guaifenesin 400 mg in 20 mL phenylephrine hydrochloride (UNII: 04JA59TNSJ) (phenylephrine - UNII:1WS297W6MV) phenylephrine hydrochloride 10 mg in 20 mL Inactive Ingredients Ingredient Name Strength 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 Color BLUE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-774-06 180 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 05/01/2018 Labeler - Wal-Mart Stores,Inc., (051957769)