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natural laxative plus stool softener

Medically reviewed on Aug 6, 2018

Dosage form: tablet
Ingredients: SENNOSIDES 8.6mg, DOCUSATE SODIUM 50mg
Labeler: McKesson (Sunmark)
NDC Code: 49348-532

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.

DRUG FACTS

Active ingredients (in each tablet)

Docusate sodium 50 mg

Sennosides 8.6 mg

Purpose

Stool softener

Laxative

Uses
  • relieves occasional constipation (irregularity)
  • generally produces bowel movement in 6-12 hours

Warnings

Do not use
  • if you are now taking mineral oil, unless directed by a doctor
  • laxative products for longer than 1 week, unless directed by a doctor

Ask a doctor before use if you have
  • stomach pain
  • nausea
  • vomiting
  • noticed a sudden change in bowel habits that continues over a period of 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 may indicate a serious condition.

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 preferably at bedtime or as directed by a doctor
 age starting dosage maximum dosage
 adults and children 12 years of age or older 2 tablets
once a day
 4 tablets
twice a day
 children 6 to under 12 years 1 tablet
once a day
 2 tablets
twice a day
 children 2 to under 6 years 1/2 tablet
once a day
 1 tablet
twice a day
 children under 2 years ask a doctor ask a doctor

Other Information
  • each tablet contains: sodium 6 mg LOW SODIUM
  • each tablet contains: Calcium 20 mg
  • store at 25o (77o F); excursions permitted between 15o- 30o C (59o-86o F)

Inactive ingredients

carnauba wax*, croscarmellose sodium, D&C yellow #10 aluminum lake, dibasic calcium phosphate dihydrate, FD&C blue #2 aluminum lake*, FD&C red #40 aluminum lake*, FD&C yellow #6 aluminum lake, hypromellose*, magnesium stearate, maltodextrin*, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol*, purified water*, silicon dioxide, sodium benzoate, stearic acid, talc*, titanium dioxide

*contains one or more of these ingredients

Questions or comments?

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

Principal Display Panel

†Compare to Senokot- S® active ingredients

Natural laxative plus stool softener

Docusate sodium 50 mg

Sennosides 8.6 mg

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

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

Another Quality Product Distributed by McKesson

One post street, San Francisco, CA 94104

Money Back Guarantee

Please visit us at www.sunmarkbrand.com

†This product is not manufactured or distributed by L.P., owner of the registered trademark Senokot-S®

Product Label

Natural laxative plus stool softener

 

NATURAL LAXATIVE  PLUS STOOL SOFTENER
docusate sodium and sennosides tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-532
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SENNOSIDES (SENNOSIDES) SENNOSIDES8.6 mg
DOCUSATE SODIUM (DOCUSATE) DOCUSATE SODIUM50 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX 
CROSCARMELLOSE SODIUM 
D&C YELLOW NO. 10 
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE 
FD&C BLUE NO. 2 
FD&C RED NO. 40 
FD&C YELLOW NO. 6 
HYPROMELLOSES 
MAGNESIUM STEARATE 
MALTODEXTRIN 
CELLULOSE, MICROCRYSTALLINE 
POLYETHYLENE GLYCOLS 
POLYVINYL ALCOHOL 
WATER 
SILICON DIOXIDE 
SODIUM BENZOATE 
STEARIC ACID 
TALC 
TITANIUM DIOXIDE 
Product Characteristics
ColorORANGEScoreno score
ShapeROUNDSize10mm
FlavorImprint CodeTCL081;SS1;S35
Contains    
Packaging
#Item CodePackage Description
1NDC:49348-532-121 BOTTLE in 1 BOX
160 TABLET 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)

 
McKesson (Sunmark)

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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