STOOL SOFTENER- docusate sodium capsule, liquid filled 
WALGREEN CO.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Walgreens 44-351

Active ingredient (in each liquid gel)

Docusate sodium 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 you have

  • 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 fail to have a bowel movement after use of a laxative. These could be signs of a serious condition
  • you need to use a laxative for more than 1 week 

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

adults and children
12 years and over 

take 1 to 3 liquid gels
daily 

children 2 to under
12 years of age
take 1 liquid gel daily 
children under
2 years of age
ask a doctor 

Other information

Inactive ingredients

D&C yellow #10, edible white ink, FD&C red #40, gelatin, glycerine, polyethylene glycol, propylene glycol, sorbitol 

Questions or comments?

1-800-426-9391

Principal display panel

Well at
Walgreens
WALGREENS PHARMACIST RECOMMENDEDǂ

NDC 0363-0351-56

STOOL SOFTENER
Gentle
Laxative
Docusate Sodium USP 100 mg 
• Gentle & easy relief of occasional constipation

25
LIQUID GELS

Compare to Dulcolax® Stool Softener Liquid Gels active ingredientǂǂ

ǂWalgreens Pharmacist Survey Study, November 2012.
ǂǂThis product is not manufactured or distributed by Boehringer Ingelheim Pharmaceuticals, Inc., owner of the registered trademark Dulcolax® Stool Softener Liquid Gels.
50844    REV0712B35156

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

Walgreens 44-351

Walgreens 44-351


STOOL SOFTENER 
docusate sodium capsule, liquid filled
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0351
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 100 mg
Inactive Ingredients
Ingredient Name Strength
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
GELATIN (UNII: 2G86QN327L)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SORBITOL (UNII: 506T60A25R)  
Product Characteristics
Color RED Score no score
Shape CAPSULE Size 13mm
Flavor Imprint Code A92
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0363-0351-56 1 in 1 CARTON
1 25 in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part334 09/21/1995
Labeler - WALGREEN CO. (008965063)
Establishment
Name Address ID/FEI Business Operations
Accucaps Industries, Ltd. 248441727 MANUFACTURE(0363-0351)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 038154464 PACK(0363-0351)

Revised: 7/2013
Document Id: 9a6a22b3-c724-4f8e-9102-2bc2d1637155
Set id: ac4e1c96-4ed3-494c-b2cf-02493a2f829d
Version: 1
Effective Time: 20130710
 
WALGREEN CO.