Mucus Relief DM Extended Release Caplets: Package Insert and Label Information

MUCUS RELIEF DM EXTENDED RELEASE CAPLETS- guaifenesin and dextromethorphan hydrobromide tablet
Walgreens

Active ingredients (in each extended-release tablet)

Dextromethorphan HBr 30 mg

Guaifenesin 600 mg

Purpose

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 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)

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 regards for timing of meals
  • adults and children 12 years of age and older: 1 or 2 tablet every 12 hours; not more than 4 tablets in 24 hours
  • children under 12 years of age: do not use

Other information

store between 20º to 25ºC (68º to 77ºF)

Inactive ingredients

carbomer, colloidal silicon dioxide, D&Cyellow #10 aluminum lake, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, povidone, talc

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal Display Panel

Compare to the active ingredients in Mucinex® DM††

12 HOUR

Mucus Relief DM

GUAIFENESIN 600 mg /

DEXTROMETHORPHAN HBr 30 mg

EXTENDED-RELEASE TABLETS

EXPECTORANT / COUGH SUPPRESSANT

12 HOUR

  • Controls Cough
  • Thins & Loosens Mucus

EXTENDED-RELEASE TABLETS

††This product is not manufactured or distributed RB Health (US) LLC, owner of the registered trademark 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: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

walgreens.com

Package Label

Dextromethorphan HBr 30 mg, Guaifenesin 600 mg
(click image for full-size original)

WALGREENS Mucus Relief DM

MUCUS RELIEF DM EXTENDED RELEASE CAPLETS
guaifenesin, dextromethorphan hbr tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0733
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GUAIFENESIN (GUAIFENESIN) GUAIFENESIN 600 mg
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE 30 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
MAGNESIUM STEARATE
CARBOMER 934
CELLULOSE, MICROCRYSTALLINE
POVIDONE
D&C YELLOW NO. 10
HYPROMELLOSE, UNSPECIFIED
LACTOSE MONOHYDRATE
TALC
Product Characteristics
Color yellow Score no score
Shape OVAL Size 16mm
Flavor Imprint Code AN038
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0363-0733-40 40 BLISTER PACK in 1 CARTON contains a BLISTER PACK
1 1 TABLET in 1 BLISTER PACK This package is contained within the CARTON (0363-0733-40)
2 NDC:0363-0733-20 20 BLISTER PACK in 1 CARTON contains a BLISTER PACK
2 1 TABLET in 1 BLISTER PACK This package is contained within the CARTON (0363-0733-20)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA209692 01/01/2019
Labeler — Walgreens (008965063)

Revised: 01/2022 Walgreens

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