UP AND UP MAXIMUM STRENGTH MUCUS RELIEF DM- dextromethorphan hydrobromide, guaifenesin tablet, extended release 
Target Corporation

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Target Corporation Maximum Strength Mucus Relief DM Drug Facts

Active ingredients (in each extended-release tablet)

Dextromethorphan HBr 60 mg

Guaifenesin 1200 mg

Purposes

Cough suppressant

Expectorant

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)

When using this product

do not use more than directed

Stop use and ask a doctor if

cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

do not crush, chew, or break tablet
take with a full glass of water
this product can be administered without regard for timing of meals
adults and children 12 years and older: 1 tablet every 12 hours; not more than 2 tablets in 24 hours
children under 12 years of age: do not use

Other information

each tablet contains: magnesium 25 mg
do not use if printed foil under cap is broken or missing
store between 20-25°C (68-77°F)

Inactive ingredients

carbomer homopolymer type B, copovidone, D&C yellow #10 aluminum lake, hypromellose, magnesium hydroxide, magnesium stearate, microcrystalline cellulose, silicon dioxide

Questions?

Call 1-888-547-7400

Package/Label Principal Display Panel

Compare to active ingredients in Maximum Strength Mucinex® DM

maximum strength mucus relief DM

guaifenesin 1200 mg

dextromethorphan hydrobromide 60 mg

extended-release tablets

expectorant and cough suppressant

controls cough

thins and loosens mucus

ACTUAL SIZE

12 HOUR

42 EXTENDED-RELEASE TABLETS

42 EXTENDED-RELEASE TABLETS

mucus relief dm image
UP AND UP MAXIMUM STRENGTH MUCUS RELIEF DM 
dextromethorphan hydrobromide, guaifenesin tablet, extended release
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-235
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN1200 mg
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE60 mg
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)  
COPOVIDONE K25-31 (UNII: D9C330MD8B)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
Product Characteristics
ColorYELLOW (light) Scoreno score
ShapeOVALSize22mm
FlavorImprint Code L812
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-235-301 in 1 CARTON09/27/2018
128 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:11673-235-661 in 1 CARTON09/27/2018
214 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:11673-235-551 in 1 CARTON04/17/2020
342 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20760209/27/2018
Labeler - Target Corporation (006961700)

Revised: 4/2020
Document Id: 617ebd8b-85db-4a79-a9b3-877f77ffa75b
Set id: 5bcb49ee-94c2-4624-824a-84213ab152b1
Version: 3
Effective Time: 20200417
 
Target Corporation