STOOL SOFTENER LAXATIVE- docusate sodium capsule, liquid filled 
Good Sense (Geiss, Destin & Dunn, Inc.)

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DRUG FACTS

Active ingredient (in each softgel)

Docusate Sodium USP, 100 mg

Purpose

Stool softener laxative

Uses

Warnings

Do not use

if you are presently taking mineral oil, unless told to do so by a doctor.

Ask a doctor before use if

  • stomach pain
  • nausea
  • vomiting
  • noticed a sudden change in bowel habits that lasts over 2 weeks


Stop use and ask a doctor if

  • you have rectal bleeding or no bowel movement after using a laxative. These could be a sign of a serious condition.
  • you need to use a laxative for more than 1 week

If pregnant or breast-feeding,

ask a health care professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center (1-800-2222-1222) right away.

Directions

adults and children 12 years and overtake 1-3 softgels daily. This dose may be taken as a single daily dose or in divided doses
children 2 to under 12 years of agetake 1 softgel daily
children under 2 years ask a doctor

Other information


Inactive ingredients

citric acid, FD&C Red #40, FD&C Yellow #6, gelatin, glycerin, polyethylene glycol, propylene glycol, purified water, sorbitol special, white edible ink


Questions or comments?

 Call  1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal Display Panel

†Compare to the active ingredient in Dulcolax® Stool Softener

Gentle

Stool Softener

Docusate Sodium 100 mg

Stool Softener Laxative

For Gentle, Softening Relief

Stimulant-free

SOFTGELS

†This product is not manufactured or distributed by Chattem, Inc., distributor of Dulcolax® Stool Softener.

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

Distributed by: Perrigo Direct, Inc.

Peachtree City, GA 30269

www.PerrigoDirect.com


Product Label

Docusate Sodium USP, 100 mg

GOOD SENSE Stool Softener Laxative

STOOL SOFTENER LAXATIVE 
docusate sodium capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50804-701(NDC:53345-008)
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
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
GELATIN (UNII: 2G86QN327L)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SORBITAN (UNII: 6O92ICV9RU)  
Product Characteristics
ColorredScoreno score
ShapeCAPSULE (Oval) Size13mm
FlavorImprint Code PC1
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50804-701-251 in 1 BOX02/03/2023
125 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00702/03/2023
Labeler - Good Sense (Geiss, Destin & Dunn, Inc.) (076059836)

Revised: 4/2024
Document Id: d3567861-6a28-4ce0-a052-68c82a36c35f
Set id: 8066a52d-e683-47c1-905c-290d2d427acf
Version: 2
Effective Time: 20240403
 
Good Sense (Geiss, Destin & Dunn, Inc.)