Mucus Relief DM Maximum Strength: Package Insert and Label Information

MUCUS RELIEF DM MAXIMUM STRENGTH- dextromethorphan hydrobromide and guaifenesin liquid
Walgreens

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active ingredients (in each 20 mL)

Dextromethorphan HBr 20 mg

Guaifenesin 400 mg

Purpose

Cough suppressant

Expectorant

Uses

  • helps loosen phelgm (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 irration 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

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 that occurs with 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 that lasts.These could be signs of a serious condition.

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 (1-800-222-1222) right away.

Directions

  • do not take more than 6 doses in any 24-hours period
  • measure only with dosing cup provided. Do not use any other dosing provided
  • keep dosing cup with product
  • dose as follows or as directed by a doctor
  • mL = milliliter
  • adults and children 12 years of age and older: 20 mL every 4 hours
  • children under 12 years of age: do not use

Other information

  • each 20 mL contains: sodium 20 mg
  • store between 20-25ºC (68-77ºF). do not refrigerate

Inactive ingredients

citric acid, disodium EDTA, FD&C red 40, flavors, glycerin, propyl gallate propylene glycol, purified water,sodium benzoate,sodium citrate, sorbitol, sucralose xanthan gum

Questions or comments?

Call 1-877-753-723-3929 Monday-Friday 9AM-5PM EST

Principal Display Panel

Compare to the active ingredients in Maximum Strength Mucinex® Fast-Max® DM Max††

DM MAX

DEXTROMETHORPHAN HBr /

COUGH SUPPRESSANT

GUAIFENESIN / EXPECTORANT

MAXIMUM STRENGTH

  • Relieves chest congestion & cough
  • Thin & loosen mucus
  • Ages 12 & over
  • 4-hour dosing

FL OZ (mL)

††This product is not manufactured or distributed by RB Health (US) LLC, owner of the registered trademarks Mucinex® Fast-Max®

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND OR UNDER CAP IS BROKEN OR MISSING.

DISTRIBUTED BY: WALGREEN CO

200 WILMOT RD., DEERFIELD, IL, 60015

walgreens.com

Package Label

Dextromethorphan HBr 20 mg, Guaifenesin 400 mg
(click image for full-size original)

WALGREENS Mucus Relief DM Maximum Strength

MUCUS RELIEF DM MAXIMUM STRENGTH
dextromethorphan hydrobromide, guaifenesin liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0505
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE 20 mg in 20 mL
GUAIFENESIN (GUAIFENESIN) GUAIFENESIN 400 mg in 20 mL
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS CITRIC ACID
WATER
SUCRALOSE
XANTHAN GUM
FD&C RED NO. 40
GLYCERIN
PROPYLENE GLYCOL
PROPYL GALLATE
SODIUM CITRATE
SODIUM BENZOATE
SORBITOL
DIBASIC CALCIUM PHOSPHATE DIHYDRATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0363-0505-06 177 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part341 08/31/2017
Labeler — Walgreens (008965063)

Revised: 02/2022 Walgreens

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