Mucus Relief Dm Tablet, Extended Release
FDA Label NDC 60000-057

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ahold U.s.a., Inc, for the product Mucus Relief Dm (NDC 60000-057). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, ask a doctor before use if you have, when using this product, stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

(in each extended-release tablet)

Dextromethorphan Hydrobromide USP 60 mg
Guaifenesin USP 1200 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 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 (1-800-222-1222) right away.

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


  • tamper evident: do not use if seal over bottle opening is broken or missing
  • store at 20° to 25°C (68° to 77°F)

Inactive Ingredients


colloidal silicon dioxide, hypromellose, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch (maize)

Questions?


call 1-877-846-9949  You may also report side effects to this phone number.

Package Label-Principal Display Panel - 1200 Mg/60 Mg (14 Tablet Bottle)

NDC 60000-057-65
CAREOne®
MUCUS RELIEF DM
Guaifenesin 1200 mg / Dextromethorphan HBr 60 mg
Extended-Release Tablets
Expectorant/Cough Suppressant

Maximum Strength
Controls Cough
Thins and Loosens Mucus
14 EXTENDED-RELEASE TABLETS    
  

Figure 1 (Guaifedextro Fig1)

Figure 1 (Guaifedextro Fig1)

Package Label-Principal Display Panel - 1200 Mg/60 Mg (14 Tablet Carton Label)

NDC 60000-057-65
CARE One®
Compare to the active ingredients
in Maximum Strength Mucinex®DM*
MUCUS
RELIEF DM
Guaifenesin 1200 mg / 
Dextromethorphan HBr 60 mg
Extended-Release Tablets
Expectorant/Cough Suppresant

Maximum Strength
Controls Cough
Thins and Loosens Mucus

14
EXTENDED-RELEASE
TABLETS


Figure 2 (Guaifedextro Fig2)

Figure 2 (Guaifedextro Fig2)


 

* Please review the disclaimer below.