MUCOSA- guaifenesin tablet

MUCOSA by

Drug Labeling and Warnings

MUCOSA by is a Otc medication manufactured, distributed, or labeled by TIME CAP LABORATORIES,INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Each immediate release tablet contains: Guaifenesin 400 mg

PURPOSE

PURPOSE: EXPECTORANT

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

INACTIVE INGREDIENT

Silicon Dioxide, Magnesium Stearate, Maltodextrin, Cellulose, Microcrystalline, Povidone, Sodium Starch Glycolate, Stearic Acid

DOSAGE & ADMINISTRATION

Adults and children 12 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 under 12 years of age do not use

INDICATIONS & USAGE

Helps loosen phlegm (mucus) and thin

bronchial secretions to make coughts more productive to rid the bronchial passageway of bothersome mucus.

WARNINGS

Ask a doctor berfoe use if you have: Persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema;  Cough accompanied by excessive phlegm (mucus)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MUCOSA 
guaifenesin tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49483-272
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)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POVIDONE (UNII: FZ989GH94E)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	white	Score	2 pieces
Shape	ROUND	Size	12mm
Flavor		Imprint Code	TCL272
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49483-272-06	60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/16/2012
2	NDC: 49483-272-00	100000 in 1 CARTON; Type 0: Not a Combination Product	04/16/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	04/16/2012

Labeler - TIME CAP LABORATORIES,INC (037052099)

Establishment
Name	Address	ID/FEI	Business Operations
TIME CAP LABORATORIES,INC		037052099	manufacture(49483-272)