Label: MAXIMUM STRENGTH MUCUS RELIEF DM- guaifenesin and dextromethorphan hbr tablet, extended release
- NDC Code(s): 0363-0510-65, 0363-0510-70, 0363-0510-99
- Packager: WALGREEN CO.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated February 3, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- 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
- for children under 12 years of age
- 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
- When using this product
- Stop use and ask a doctor if
- If pregnant or breast-feeding,
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- Questions?
-
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 1200 mg/60 mg (14 Tablet Carton Label)
NDC 0363-0510-65
Walgreens
Compare to the active ingredients in
Maximum Strength Mucinex® DM††
WALGREENS
PHARMACIST RECOMMENDED
12 HOUR
Mucus
Relief DM
GUAIFENESIN 1200 mg / EXPECTORANT
DEXTROMETHORPHAN HBr 60 mg /
COUGH SUPPRESSANT
EXTENDED-RELEASE TABLETS
Maximum Strength 12 Hour- Controls cough
- Thins & loosens mucus
14
EXTENDED-
RELEASE
TABLETS
ACTUAL SIZE
-
INGREDIENTS AND APPEARANCE
MAXIMUM STRENGTH MUCUS RELIEF DM
guaifenesin and dextromethorphan hbr tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0510 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 1200 mg DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 60 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POVIDONE K90 (UNII: RDH86HJV5Z) POVIDONE K25 (UNII: K0KQV10C35) STARCH, CORN (UNII: O8232NY3SJ) Product Characteristics Color WHITE (white to off-white) Score no score Shape OVAL Size 22mm Flavor Imprint Code X;63 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0510-65 2 in 1 CARTON 03/17/2017 1 7 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0363-0510-70 4 in 1 CARTON 03/17/2017 2 7 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:0363-0510-99 6 in 1 CARTON 03/17/2017 3 7 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA206941 03/17/2017 Labeler - WALGREEN CO. (008965063) Registrant - Aurohealth LLC (078728447) Establishment Name Address ID/FEI Business Operations Aurobindo Pharma Limited 650381903 ANALYSIS(0363-0510) , MANUFACTURE(0363-0510)