MUCUS RELIEF GUAIFENESIN EXTENDED-RELEASE 600 MG- guaifenesin tablet 
TWIN MED LLC

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TWIN MED - PROCURE - MUCUS RELIEF (GUAIFENESIN EXTENDED-RELEASE) TABLETS, 600 MG (55681-301)

Active ingredient (in each extended-release tablet)

GUAIFENESIN 600 MG

PURPOSE

EXPECTORANT

Uses

Warnings

Do not use

Ask a doctor before use if you have

Stop use and ask a doctor if

If pregnant or breast-feeding, ask a health 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

Inactive ingredients

carbomer homopolymer type B, hypromellose, magnesium stearate, microcrystalline cellulose, sodium starch glycolate.

Questions?

call toll-free 1-800-935-6737

PDP

DF1

DF2

MUCUS RELIEF  GUAIFENESIN EXTENDED-RELEASE 600 MG
guaifenesin tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55681-301
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN600 mg
Inactive Ingredients
Ingredient NameStrength
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
Product Characteristics
ColorwhiteScoreno score
ShapeOVALSize16mm
FlavorImprint Code G;600
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55681-301-01100 in 1 BOTTLE; Type 0: Not a Combination Product03/02/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21342003/02/2022
Labeler - TWIN MED LLC (009579330)

Revised: 1/2024
Document Id: 0e12d44c-f957-c1b1-e063-6394a90a7483
Set id: d9d13c67-51a1-aa79-e053-2995a90abdbb
Version: 2
Effective Time: 20240103
 
TWIN MED LLC