NDC | 11673-834-14, 11673-834-28 |
Set ID | ad93badc-37bc-48eb-ad84-e4966d63d877 |
Category | HUMAN OTC DRUG LABEL |
Packager | TARGET Corporation |
Generic Name | |
Product Class | |
Product Number | |
Application Number | ANDA209692 |
- Active ingredients (in each extended-release tablets )
- Purpose
-
Uses
- help 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?
-
Principal Display Panel
Compare to active ingredients in Maximum Strength Mucinex® DM*
Maximum Strength
mucus relief DM
guaifenesin 1,200 mg
expectorant
dextromethorphan HBr 60 mg
cough suppressant
controls cough
thins and loosens mucus
EXTENDED-RELEASE TABLETS
*This product is not manufactured or distributed by Reckitt Benckiser, distributor of Maximum Strength 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.
Distributed by Target Corporation
Minneapolis, MN 55403
TM & ©2018 Target Brands, Inc.
- Package Label
-
INGREDIENTS AND APPEARANCE
MUCUS RELIEF DM MAX MAXIMUM STRENGTH
dextromethorphan hbr, guaifenesin tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-834 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 60 mg GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 1200 mg Inactive Ingredients Ingredient Name Strength CARBOMER 934 (UNII: Z135WT9208) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POVIDONE (UNII: FZ989GH94E) TALC (UNII: 7SEV7J4R1U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color YELLOW Score no score Shape OVAL Size 22mm Flavor Imprint Code AN039 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-834-28 28 in 1 CARTON 01/01/2019 12/30/2022 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:11673-834-14 14 in 1 CARTON 01/01/2019 12/30/2022 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 01/01/2019 12/30/2022 Labeler - TARGET Corporation (006961700)