NDC | 37012-730-20, 37012-730-40 |
Set ID | 369cdb35-6380-4ef0-bc77-15baf2bc8205 |
Category | HUMAN OTC DRUG LABEL |
Packager | Shopko Stores Operating Co., LLC. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | ANDA209692 |
- Active ingredients (in each extended-release tablet)
- 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 under12 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 or comments?
-
Principal Display Panel
*Compare to Mucinex® DM active ingredients
MUCUS RELIEF DM
GUAIFENESIN 600 mg
Expectorant HBr 30 mg
DEXTROMETHORPHAN HBr 30 mg
Expectorant
Cough suppressant
12-hour relief
Controls cough
Thins and Loosens mucus
EXTENDED-RELEASE TABLETS
*This product is not manufactured or distributed Reckitt Benckiser LLC, distributor of Mucinex® DM.
TAMPER EVIDENT: DO NOT USE IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
Packaged by: PL Developments
200 Hicks Street, Westbury, NY 11590, USA
©2018 Shopko Stores, Operating Co., LLC
- Package Label
-
INGREDIENTS AND APPEARANCE
MUCUS RELIEF DM EXTENDED RELEASE CAPLETS
guaifenesin, dextromethorphan hbr tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37012-730 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 SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MAGNESIUM STEARATE (UNII: 70097M6I30) CARBOMER 934 (UNII: Z135WT9208) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POVIDONE (UNII: FZ989GH94E) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) TALC (UNII: 7SEV7J4R1U) Product Characteristics Color YELLOW Score no score Shape OVAL Size 16mm Flavor Imprint Code AN038 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37012-730-20 20 in 1 CARTON 01/04/2019 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:37012-730-40 40 in 1 CARTON 01/04/2019 2 1 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 ANDA209692 01/04/2019 Labeler - Shopko Stores Operating Co., LLC. (023252638)