STOOL SOFTENER DOCUSATE SODIUM- docusate sodium capsule, gelatin coated 
Magno-Humphries, Inc.

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Stool Softener Docusate Sodium

MHL NDC 54257-902-06

Stool Softener Docusate Sodium 100mg Compare to the active ingredient in Colace *


®

Effective, Gentle Stimulant Free For Comfortable Relief


1000 SOFTGELS

DO NOT USE IF PRINTED SEAL UNDER CAP IS MISSING OR DAMAGED

Active ingredient (in each softgel)

Docusate sodium 100mg

Purpose

Stool softener

Uses

Warnings

​Do not use

​Ask a doctor before use if you have

​Stop use and ask a doctor if

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

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

FD&C red #40, FD&C yellow #6, gelatin, glycerin, polyethylene glycol 400, purified water, sorbitol.

Questions?

call toll-free ​1-800-935-6737

*This product is not manufactured or distributed by the owner of the registered trademark Colace®. Distributed by: Magno-Humphries, Inc. OR 97223 U.S.A. ​Visit our website: www.magno-humphries.com






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

Distributed by: , OR 97223 U.S.A.



Magno-Humphries, Inc.​Visit our website: www.magno-humphries.com

Package Labeling:

Label

Drug Facts

STOOL SOFTENER DOCUSATE SODIUM 
docusate sodium capsule, gelatin coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54257-902
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
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
Product Characteristics
ColorredScoreno score
ShapeOVALSize12mm
FlavorImprint Code SCU1
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54257-902-061000 in 1 BOTTLE; Type 0: Not a Combination Product04/04/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00704/04/2017
Labeler - Magno-Humphries, Inc. (063251433)

Revised: 10/2023
Document Id: 08bf67ab-e837-2223-e063-6294a90a0878
Set id: a0e6ab9b-fd31-45fd-93d5-b51d705c180a
Version: 5
Effective Time: 20231027
 
Magno-Humphries, Inc.