DOCUSATE SODIUM- docusate sodium capsule 
Cellchem Pharmaceutical Inc

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Active Ingredient (in each capsule)                         Purpose

Docusate sodium 100 mg................................................Laxative, stool softener

Stool Softener

Uses

Warnings


Do not use

  • if you have
    • abdominal pain
    • nausea
    • fever
    • vomiting
  • with other medicines or if you are presently taking mineral oil
  • if you are on a low salt diet
  • longer than 7 days

When using this product

  • frequent or prolonged use may result in dependence on laxatives
  • it may take up to 3 days for you to have a bowel movement

Stop use and ask a doctor if

  • rectal bleeding occurs
  • symptoms persist, last for more than 7 days

Keep out of reach of children. In case of overdose, call a poison control centre or get medical help right away, even if you do not notice any signs or symptoms. 

Directions

Other information

1(844) 481-8884

Inactive ingredients

Polyethylene glycol 400, propylene glycol, gelatin, glycerin, sodium methyl paraben, sodium propyl paraben, sorbitol sorbitan solution, purified water, FD&C Red No. 40, FD&C Yellow No. 6.

Manufactured for :
CellChem Pharmaceuticals Inc.
Ottawa, ON, Canada K2E 7V7

label

DOCUSATE SODIUM 
docusate sodium capsule
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73147-8273
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM100 mg
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GELATIN (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)  
PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)  
SORBITOL SOLUTION (UNII: 8KW3E207O2)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Colorred (Dark Red) Scoreno score
ShapeOVALSize15mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73147-8273-1100 in 1 BOTTLE; Type 0: Not a Combination Product10/10/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00710/10/2023
Labeler - Cellchem Pharmaceutical Inc (111518618)
Establishment
NameAddressID/FEIBusiness Operations
Softgel Healthcare Private Limited675584180manufacture(73147-8273)

Revised: 12/2023
Document Id: 2b0cb99e-f6cb-412d-9784-49fa5653ead8
Set id: 027bfef9-f46c-4ddc-b65a-26f1b0b81a75
Version: 2
Effective Time: 20231221
 
Cellchem Pharmaceutical Inc