SENNOSIDES, DOCUSATE SODIUM- sennosides, docusate sodium tablet, film coated 
CVS Pharmacy, Inc.

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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0490C-CVS

Drug Facts

Active Ingredients (in each tablet)

Docusate sodium 50 mg

Sennosides 8.6 mg

Purpose

Stool softener and 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
    agestarting dosagemaximum dosage

    adults and children

    12 years of age and over

    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: calcium 11 mg 
  • each tablet contains: sodium 4 mg 
  • store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)

croscarmellose sodium, dicalcium phosphate, FD&C yellow #5 lake*, FD&C yellow #6 lake, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, mineral oil, polyethylene glycol, sodium benzoate, sodium lauryl sulfate, starch, stearic acid, talc, titanium dioxide, triacetin

*contains FD&C yellow #5 lake (tartrazine) as a color additive.

Questions or comments?

Call 1-800-231-4670 Monday - Friday 9AM-5PM EST

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

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

†This product is not manufactured or distributed by Purdue Products L.P., distributor of Senokot-S®.

Distributed by: CVS Pharmacy, Inc.

One CVS Drive, Woonsocket, RI 02895

© 2018 CVS/pharmacy

CVS.com® 1-800-SHOP CVS

V-30287

CVSHealth

Compare to the active ingredients in Senokot-S®†

Senna Plus

DOCUSATE SODIUM, 50 mg

SENNOSIDES, 8.6 mg

Laxative/Stool softener

Natural vegetable laxative ingredient plus stool softener

30 TABLETS

0490C

SENNOSIDES, DOCUSATE SODIUM 
sennosides, docusate sodium tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-409
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM50 mg
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES8.6 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIACETIN (UNII: XHX3C3X673)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
ColoryellowScoreno score
ShapeROUNDSize10mm
FlavorImprint Code CPC;490
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-409-301 in 1 CARTON07/03/201810/31/2021
130 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:69842-409-06180 in 1 BOTTLE; Type 0: Not a Combination Product07/03/201810/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33407/03/201810/31/2021
Labeler - CVS Pharmacy, Inc. (062312574)

Revised: 11/2020
Document Id: b454656f-769f-6b11-e053-2a95a90a4a68
Set id: 6dd74330-383c-0a77-e053-2991aa0a1817
Version: 3
Effective Time: 20201117
 
CVS Pharmacy, Inc.