Label: MUCINEX DM, CVP HEALTH- guaifenesin and dextromethorphan hydrobromide tablet, extended release
MUCINEX DM, TRAVEL BASIX- guaifenesin and dextromethorphan hydrobromide tablet, extended release
MUCINEX DM- guaifenesin and dextromethorphan hydrobromide tablet, extended release
- NDC Code(s): 66715-6424-1, 66715-6524-1, 66715-9724-1
- Packager: Lil' Drug Store Products, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 10, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
-
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
- persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
- cough accompanied by too much phlegm (mucus)
- Directions
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- Mucinex ® DM 2ct, Lil' Drug Store ® - PDP/Package
-
Mucinex
® DM 2ct, TRAVEL BASIX - PDP/Package
Mucinex ® DM
600 mg guaifenesin & 30 mg dextromethorphan HBr
extended-release bi-layer tablets
EXPEXTORANT & COUGH SUPPRESSANT
12
HOUR
[tablet image]
[check mark] Controls Cough
[check mark] Thins and Loosens Mucus
[check mark] Immediate and Extended release
2
EXTENDED-RELEASE
BI-LAYER TABLETS
[TRAVEL BASIX logo]
®
-
Mucinex
® DM 2ct CVP
® HEALTH - PDPPackage
Mucinex ® DM
600 mg guaifenesin & 30 mg dextromethorphan HBr
extended-release bi-layer tablets
EXPEXTORANT & COUGH SUPPRESSANT
12
HOUR
[tablet image]
[check mark] Controls Cough
[check mark] Thins and Loosens Mucus
[check mark] Immediate and Extended release
2
EXTENDED-RELEASE
BI-LAYER TABLETS
[CVP ® HEALTH logo]
-
INGREDIENTS AND APPEARANCE
MUCINEX DM, CVP HEALTH
guaifenesin and dextromethorphan hydrobromide tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66715-6524 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 600 mg DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 30 mg Inactive Ingredients Ingredient Name Strength SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) ALUMINUM OXIDE (UNII: LMI26O6933) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) Product Characteristics Color white (Yellow and white) Score no score Shape OVAL Size 16mm Flavor Imprint Code Mucinex;600 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66715-6524-1 1 in 1 CARTON 05/06/2022 1 2 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA021620 05/06/2022 MUCINEX DM, TRAVEL BASIX
guaifenesin and dextromethorphan hydrobromide tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66715-6424 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 600 mg DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 30 mg Inactive Ingredients Ingredient Name Strength SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) ALUMINUM OXIDE (UNII: LMI26O6933) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) Product Characteristics Color white (Yellow and white) Score no score Shape OVAL Size 16mm Flavor Imprint Code Mucinex;600 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66715-6424-1 1 in 1 CARTON 11/29/2022 1 2 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA021620 11/29/2022 MUCINEX DM
guaifenesin and dextromethorphan hydrobromide tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66715-9724 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 600 mg DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 30 mg Inactive Ingredients Ingredient Name Strength MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) ALUMINUM OXIDE (UNII: LMI26O6933) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color white (Yellow and white) Score no score Shape OVAL Size 16mm Flavor Imprint Code Mucinex;600 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66715-9724-1 1 in 1 CARTON 05/10/2010 1 2 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA021620 05/10/2010 Labeler - Lil' Drug Store Products, Inc. (093103646)