OTC Medication Information: CVS Mucus Relief DM Maximum Strength

CVS MUCUS RELIEF DM MAXIMUM STRENGTH- dextromethorphan hydrobromide and guaifenesin solution
CVS PHARMACY

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.

Drug Facts

Active ingredients
(in each 20 mL)
Purposes

Dextromethorphan HBr 20 mg

Cough suppressant

Guaifenesin 400 mg

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

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 right away at 1-800-222-2222.

Directions

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

Other information

each 20 mL contains: sodium 8 mg
low sodium
store at room temperature
do not refrigerate
dosing cup provided

Inactive ingredients

anhydrous citric acid, edetate disodium, FD&C Blue No. 1, FD&C Red No. 40, flavors, potassium citrate , propylene glycol, propyl gallate, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum.

Questions or comments?

1-866-467-2748

PRINCIPAL DISPLAY PANEL

NDC# 69842-937-06

*Compare to Maximum Strength Mucinex® Fast-Max® DM max active ingredients††

DM Max

DEXTROMETHORPHAN HBr/ COUGH SUPPRESSANT
GUAIFENESIN 400 mg/ EXPECTORANT

MAXIMUM STRENGTH

MULTI-SYMPTOM

Relieves Chest Congestion & cough
Thins & Loosens Mucus
4 Hour Dosing
12 years & older

For Ages 12+

6 FL OZ (180 mL)

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

DISTRIBUTED BY:

WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

100% SATISFACTION GUARANTEED

Walgreens.com © 2020 Walgreen Co.

*This product is not manufactured or distributed by Reckitt Benckiser, the distributor of Maximum Strength Mucinex® Fast -Max® DM Max.

CVS Mucus Relief DM Maximum Strength
(click image for full-size original)
CVS MUCUS RELIEF DM MAXIMUM STRENGTH
dextromethorphan hbr and guaifenesin solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-937
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
edetate disodium
FD&C BLUE NO. 1
FD&C red No. 40
POTASSIUM CITRATE
propylene glycol
propyl gallate
water
sodium benzoate
sorbitol
sucralose
xanthan gum
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:69842-937-06 180 mL in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part341 03/30/2020
Labeler — CVS PHARMACY (062312574)

Revised: 06/2022 CVS PHARMACY

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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