MUCUS RELIEF- guaifenesin 400 mg tablet

MUCUS RELIEF by

Drug Labeling and Warnings

MUCUS RELIEF by is a Otc medication manufactured, distributed, or labeled by Pioneer Life Sciences, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Guaifenesin 400 mg

Purpose

Expectorant

Uses

• helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and makes coughs more productive

Warnings

Do not use: for children under 12 years of age

Ask a doctor before use if you have

• persistent cough such as occurs with smoking, asthma, chronic bronchitis or emphysema
• cough is accompanied by too much phlegm (mucus)

Stop use and ask a doctor if

• cough lasts for more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious condition.

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding,ask a health care professional before use.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

• Adults and children 12 years 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 under 12 years:do not use

Other information

• Store at 25°C (77°F) excursions between 15°-30°C (59°-86°F)
• Keep in a dry place and do not expose to heat
• Read all product information before using

Inactive ingredients

Colloidal Silicon Dioxide, Croscarmellose Sodium, Magnesium Stearate, Maize Starch, Microcrystalline Cellulose, Povidone K-30, Sodium Lauryl Sulphate

Questions or Comments ?

Call 1-732-698-5070 Monday through Friday 9 am to 5 pm EST 

SPL UNCLASSIFIED SECTION

This product is not manufcatured or distributed by Reckitt Benckiser's , owner of the Registered Trademark MUCINEX®

SPL UNCLASSIFIED SECTION

Distributed by: GenCare Consumer Products, LLC

40E Cotters Ln Suite A, East Brunswick, NJ 08816

PRINCIPAL DISPLAY PANEL

NDC 72090-013-01

INGREDIENTS AND APPEARANCE

MUCUS RELIEF 
guaifenesin 400 mg tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72090-013
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
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
STARCH, CORN (UNII: O8232NY3SJ)
POVIDONE K30 (UNII: U725QWY32X)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)

Product Characteristics
Color	white	Score	no score
Shape	capsule	Size	17mm
Flavor		Imprint Code	GT
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72090-013-01	200 in 1 BOTTLE; Type 0: Not a Combination Product	01/19/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	01/19/2024

Labeler - Pioneer Life Sciences, LLC (014092742)