MUCUS RELIEF IMMEDIATE RELEASE- mucus relief tablet

Mucus Relief by

Drug Labeling and Warnings

Mucus Relief by is a Otc medication manufactured, distributed, or labeled by Allegiant Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

• 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

• do not use if imprinted safety seal under cap is broken or missing
  

Storage

• store at 25°C (77°F) excursions between 15° to 30°C (59° to 86°F)
• keep in a dry place and do not expose to heat
  

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

INGREDIENTS AND APPEARANCE

MUCUS RELIEF  IMMEDIATE RELEASE
mucus relief tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69168-916
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	400 mg

Inactive Ingredients
Ingredient Name	Strength
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
Color	white	Score	2 pieces
Shape	OVAL	Size	17mm
Flavor		Imprint Code	AZ370
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69168-916-60	1 in 1 CARTON	04/19/2021
1		60 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	12/23/2014

Labeler - Allegiant Health (079501930)