DULCOLAX PINK STOOL SOFTENER- docusate sodium capsule, liquid filled 
Chattem, Inc.

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Dulcolax Pink Stool Softener

Dulcolax Pink®

Stool Softener

Drug Facts

Active ingredient (in each capsule) 

Docusate sodium (USP) 100 mg

Purpose

Stool softener laxative

Use

● for relief of occasional constipation and irregularity

this product generally produces bowel movement in 12 to 72 hours

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 or vomiting

● a sudden change in bowel habits that lasts more than 2 weeks

Stop use and ask a doctor if

 you have rectal bleeding or no bowel movement after using this product. 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 right away.

Directions

take with a glass of water

adults and children 12 years of age and over       1 to 3 capsules daily. This dose may be taken as a single daily dose or in divided doses.

children 2 to under 12 years of age                         1 capsule daily

children under 2 years of age                               ask a doctor

Other information

 each capsule contains: sodium 6 mg

● store at 20°-25°C (68°-77°F)

● protect from excessive humidity

● do not use this product if the safety seal under the cap is torn or missing

Inactive ingredients

D&C red no. 33, FD&C blue no. 1, FD&C red no. 40, FD&C yellow no. 6, gelatin, glycerin, mannitol, pharmaceutical ink, polyethylene glycol 400, propylene glycol, sorbitan, sorbitol, titanium dioxide, water

Questions?

Call 1-866-844-2798 or visit www.Dulcolax.com

PRINCIPAL DISPLAY PANEL

Dulcolax
Pink
STOOL SOFTENER
25 SOFTGELS

PRINCIPAL DISPLAY PANEL
Dulcolax
Pink
STOOL SOFTENER
25 SOFTGELS

DULCOLAX PINK STOOL SOFTENER 
docusate sodium capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0281
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
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
GELATIN (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
MANNITOL (UNII: 3OWL53L36A)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SORBITAN (UNII: 6O92ICV9RU)  
SORBITOL (UNII: 506T60A25R)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Colorred, whiteScoreno score
ShapeOVALSize13mm
FlavorImprint Code L486
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41167-0281-11 in 1 CARTON02/18/2018
125 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:41167-0281-21 in 1 CARTON09/07/2018
230 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)02/18/2018
Labeler - Chattem, Inc. (003336013)

Revised: 11/2023
Document Id: ee31e609-02c9-4127-a6ad-77c141c1ed49
Set id: 33fefcf1-9985-4797-9a38-8acaf3979fce
Version: 5
Effective Time: 20231103
 
Chattem, Inc.