MUCOSA- guaifenesin tablet 
TIME CAP LABORATORIES,INC

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272R Timely 49483-272 Guaifenesin 400 mg Tablets

Active ingredient (in each immediate-release tablet)

Guaifenesin 400 mg

Purpose

Expectorant

Uses

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.

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

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

Directions

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

Inactive ingredients colloidal silicon dioxide, magnesium stearate, maltodextrin, microcrystalline cellulose, povidone, silicon dioxide, sodium starch glycolate, stearic acid

Questions or comments?

Call 1-877-290-4008

272R-Timely-200s-labelimage description60lable

MUCOSA 
guaifenesin tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49483-272
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg
Inactive Ingredients
Ingredient NameStrength
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
ColorwhiteScore2 pieces
ShapeROUNDSize12mm
FlavorImprint Code TCL272
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49483-272-0660 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/16/2012
2NDC:49483-272-00100000 in 1 CARTON; Type 0: Not a Combination Product04/16/2012
3NDC:49483-272-20200 in 1 BOTTLE; Type 0: Not a Combination Product09/15/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01204/16/2012
Labeler - TIME CAP LABORATORIES,INC (037052099)
Registrant - TIME CAP LABORATORIES,INC (037052099)
Establishment
NameAddressID/FEIBusiness Operations
TIME CAP LABORATORIES,INC037052099manufacture(49483-272)

Revised: 11/2023
Document Id: 092526a7-c2e1-4cb5-e063-6394a90ac509
Set id: d34ef2e8-adc2-48e5-a572-e354937daec6
Version: 5
Effective Time: 20231102
 
TIME CAP LABORATORIES,INC