MUCUS RELIEF IMMEDIATE RELEASE- mucus relief tablet 
Allegiant Health

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Sound Body Mucus Relief

Active ingredient(s)

Guaifenesin 400 mg

Purpose

Expectorant

Use(s)

Warnings

Ask a doctor before use if

  • 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 caplet every 4 hours with a full of glass of water while symptoms persist. Do not exceed 6 doses in 24 hours.

Children under 12 years of age: do not use

Other information

Storage

Inactive ingredients

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

Questions

Call 1-888-952-0050

Monday through Friday 9AM - PM EST.

Principal Display Panel

Mucus Relief

Mucus Relief

MUCUS RELIEF  IMMEDIATE RELEASE
mucus relief tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69168-916
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)  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
POVIDONE (UNII: FZ989GH94E)  
Product Characteristics
ColorwhiteScore2 pieces
ShapeOVALSize17mm
FlavorImprint Code AZ370
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69168-916-601 in 1 CARTON04/19/2021
160 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01212/23/2014
Labeler - Allegiant Health (079501930)

Revised: 4/2021
Document Id: 133e0907-41f5-497d-bc1e-3e227ba978b7
Set id: 237f7d7a-f394-4795-980c-3d71efe2cccc
Version: 4
Effective Time: 20210419
 
Allegiant Health