GUAIFENESIN- guaifenesin liquid 
KESIN PHARMA CORPORATION

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Guaifenesin Oral Solution, USP

Drug Facts

Active ingredient (in each 5 mL teaspoonful)

Guaifenesin, USP 100 mg

Purpose

Expectorant

Uses

Warnings

Do not use

  • if you ever had an allergic reaction to any of the ingredients in this product

Ask a doctor before use if you have

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

Stop use and ask a doctor if

cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistant headache. These could be signs of a serious condition.

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 right away.

Directions

AgeDose
adults and children 12 years and over2 to 4 tespoonfuls every 4 hours
children 6 years to under 12 years1 to 2 teaspoonfuls every 4 hours
children 2 years to under 6 years1/2 to 1 teaspoonful every 4 hours
under 2 yearsask a doctor

Other information

Inactive ingredients

citric acid, grape flavor, methylparaben, monoammonium glycyrrhizinate, potassium citrate, propylene glycol, propylparaben, purified water, sorbitol, sucralose

Questions or comments?

1-833-537-4679

*This product is not manufactured or distributed by the owner of registered trademark of Robitussin ®.

Distributed by:

Kesin Pharma

Oldsmar, FL 34677

Revision 03/2025

Kesin Pharma Logo

NDC 81033-102-16

Guaifenesin Oral Solution, USP

100 mg/5 mL

Expectorant

Grape Flavor

16 fl oz (473 mL)

Guaifenesin 16 oz Bottle Label

GUAIFENESIN 
guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81033-102
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
POTASSIUM CITRATE ANHYDROUS (UNII: 86R1NVR0HW)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
SORBITOL (UNII: 506T60A25R)  
CITRIC ACID (UNII: 2968PHW8QP)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81033-102-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01204/01/2025
Labeler - KESIN PHARMA CORPORATION (117447816)
Establishment
NameAddressID/FEIBusiness Operations
Kesin Pharma117447816pack(81033-102) , label(81033-102)

Revised: 4/2025
Document Id: 31b88302-3352-a500-e063-6294a90acce8
Set id: 31b8ad0a-3637-03db-e063-6394a90acdc3
Version: 1
Effective Time: 20250401
 
KESIN PHARMA CORPORATION