MUCUS RELIEF IMMEDIATE RELEASE- guaifenesin 400mg tablet 
TopCo Associates, LLC

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370- Mucus Relief

Active ingredient(s)

Guaifenesin 400 mg

Purpose

Expectorant

Use(s)

helps loosen phlegm (mucus)and thin bronchial secretions to make
coughs more productive to rid the bronchial passageway of bothersome mucus

Warnings

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 excessive phlegm (mucus)

When using this product

  • do not exceed recommended dosage
  • do not use for more than 7 days

Stop use and ask a doctor if

  • cough lasts for more than 7 days, recurs, or is
    accompanied by fever, rash, or persistent
    headache. These could be signs of a
    serious condition.

Pregnancy/Breastfeeding

ask a healthcare professional before use.

Keep out of reach of children

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

Directions

Adults and children12 years of age and older Take 1 tablet every 4 hours with a full glass of water while symptoms persist. Do not exceed 6 doses in 24 hours.

Children under12 years of age:  do not use

Other information

Storage

Inactive ingredients

Croscarmellose Sodium, Maltodextrin, Microcrystalline Cellulose, Povidone, Silicon Dioxide, Stearic Acid

Questions

Call 1-888-423-0139

Principal Display Panel

Mucus Relief

Mucus Relief

MUCUS RELIEF  IMMEDIATE RELEASE
guaifenesin 400mg tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76162-004
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
POVIDONE (UNII: FZ989GH94E)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
Product Characteristics
ColorwhiteScore2 pieces
ShapeOVALSize17mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76162-004-812 in 1 CARTON12/23/201401/31/2022
1200 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:76162-004-01100 in 1 BOTTLE; Type 0: Not a Combination Product12/23/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01212/23/2014
Labeler - TopCo Associates, LLC (006935977)

Revised: 1/2021
Document Id: bf64ce65-6978-4634-bd02-ab1389acf47d
Set id: 7d91c6ab-d161-42b9-b353-0aa8f59619f8
Version: 7
Effective Time: 20210121
 
TopCo Associates, LLC