STOOL SOFTENER- docusate sodium capsule, liquid filled 
Mckesson (Sunmark)

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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Drug Facts

Active Ingredient (in each softgel)

Docusate Sodium 100 mg

Purpose

Stool softener

Uses

Warnings - Do not use

Ask a doctor before use if

you notice a sudden change in bowel habits that persists over a period of 2 weeks

Stop use and ask a doctor if

  • you have rectal bleeding
  • you fail to have a bowel movement after use

If pregnant or breastfeeding

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 right away.

Directions

Other information

Inactive Ingredients

edible ink, D&C Red #33, FD&C Red #40, FD&C Yellow #6, gelatin, glycerin, polyethylene glycol, propylene glycol, sorbitol special and titanium dioxide. May also contain: FD&C blue #1 and purified water.

Principal Display Panel

Compare to COLACE® active ingredient*

stool softener

Relief of occasional constipation

Docusate sodium 100 mg

Another quality product distributed by McKesson

one post street

San Francisco, CA 94104

Money back gurantee

Please visit us at www.sunmarkbrand.com

Product Label

Sunmark stool softener

Docusate Sodium 100 mg

 

STOOL SOFTENER 
docusate sodium capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:49348-616
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DOCUSATE SODIUM (DOCUSATE) DOCUSATE SODIUM100 mg
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 
FD&C YELLOW NO. 6 
GELATIN 
GLYCERIN 
POLYETHYLENE GLYCOLS 
PROPYLENE GLYCOL 
SORBITOL 
D&C RED NO. 33 
TITANIUM DIOXIDE 
FD&C BLUE NO. 1 
WATER 
Product Characteristics
ColorRED, WHITEScoreno score
ShapeOVALSize13mm
FlavorImprint Code P10;51A
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49348-616-101 in 1 BOX
1100 in 1 BOTTLE
2NDC:49348-616-90400 in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart33407/09/2010
Labeler - Mckesson (Sunmark) (177667227)

Revised: 9/2012
Document Id: 32e8158b-51f5-48bd-9058-3c49f9af23a4
Set id: 5d117378-8322-42dd-846c-932590ae752c
Version: 1
Effective Time: 20120924
 
Mckesson (Sunmark)