Label: MUCUS RELIEF DM MAX- dextromethorphan hbr, guaifenesin solution
- NDC Code(s): 55910-146-95
- Packager: DOLGENCORP, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 10, 2024
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- Official Label (Printer Friendly)
- Active ingredients (in each 20 mL)
- Purpose
-
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)
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal display panel
DG™ | health
Compare to active
ingredients of
Maximum Strength
Mucinex® FAST-MAX®
DM MAX*Maximum Strength
Mucus Relief
DM MaxDextromethorphan HBr
Cough Suppressant
Guaifenesin
Expectorant• Controls cough
• Relieves chest congestion
• Thins & loosens mucus
• 4-hour dosingFor Ages 12 Years & Over
9 FL OZ (266 mL)
DISTRIBUTED BY
OLD EAST MAIN CO.
100 MISSION RIDGE
GOODLETTSVILLE, TN 37072PARENTS:
Learn about teen medicine abuse
www.StopMedicineAbuse.org100%
Satisfaction
Guaranteed!
(888) 309-9030*This product is not manufactured or distributed by
RB Health (US) LLC, owner of the registered
trademark Maximum Strength Mucinex® FAST-MAX®
DM MAX. 50844 ORG042403195
Dollar General 44-031A
-
INGREDIENTS AND APPEARANCE
MUCUS RELIEF DM MAX
dextromethorphan hbr, guaifenesin solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-146 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 Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K) SORBITOL SOLUTION (UNII: 8KW3E207O2) SUCRALOSE (UNII: 96K6UQ3ZD4) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color red Score Shape Size Flavor BERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-146-95 266 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/07/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 10/07/2024 Labeler - DOLGENCORP, LLC (068331990) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 manufacture(55910-146) , pack(55910-146)