SENEXON-S- docusate sodium -sennosides tablet, coated 
Cardinal Health

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 ingredients (in each tablet) Purposes

Docusate sodium 50 mg . . . . . . . . . . .Stool Softener

Sennosides 8.6 mg. . . . . . . . . . . . . . . .Stimulant Laxative

Natural Vegetable Stimulant

Laxative Plus Stool Softener

ASK A DOCTOR BEFORE USE IF YOU HAVE A SUDDEN CHANGE IN BOWEL HABITS THAT LASTS OVER TWO WEEKS

Ask a doctor or pharmacist before use if you are taking any other drug.  Laxatives may affect how other drugs work.

Do not use if your are taking mineral oil; for longer than one week; when abdominal pain, nausea or vomiting are present

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

If pregnant or breast-feeding, ask a health professional before use.

Uses:  relieves occasional constipation; generally produces bowel movement in  6-12 hours.

Questions or comments? 1-800-645-2158

Stop use and ask a doctor if: you have rectal bleeding; you fail to have a bowel movement after use of this product.  These may indicate a serious condition.

Inactive ingredients

carnauba wax, colloidal silicon dioxide, croscarmellose sodium

D&C yellow #10 aluminum lake, dibasic calcium phosphate

dihydrate, FD-C yellow #6 aluminum lake, hypromellose,

magnesium stearate, microcrystalline cellulose, polyethylene

glycol, sodium benzoate, stearic acid, titanium dioxide

Directions

take preferably at bedtime or as directed by a doctor

If you do not have a comfortable bowel movement by the second day, increase dose by one tablet (do not exceed maximum dosage)

 
Dosage and Administration

Adults and children 12 years and over - 2 tablets once daily - maximum dosage - 4 tablets twice daily

children 6 to under 12 years - 1 tablet once daily - maximum dosage - 2 tablets twice daily

children 2 to under 6 years - 1/2 tablet once daily - maximum dosage- 1 tablet twice daily

children under 2 years - ask a doctor

RELIEVES OCCASIONAL CONSTIPATION

GENERALLY PRODUCES BOWEL MOVEMENT IN 6-12 HOURS

Dispense contents with a child-resistant closure in a tight, light-resistant container as defined in the USP.

Each tablet contains: calcium 20 mg, sodium 6 mg (LOW SODIUM)

Store at 20-25C° (68-77F°)

*Rugby Laboratories is not affiliated with the owner of registered trademark Senokot-S®

Distributed by : Rugby Laboratories

31778 Enterprise Drive, Livonia, MI 48150

Repackaged By:

Cardinal Health

Zanesville, OH 43701

Rev. 03/13

IT49413241113

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Senexon-S Tablets

28 day card label

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Senexon-S 50/8.6 mg TB, 28s

28 day lidding label

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Senexon-S Tablets

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Senexon-S Tablets

QTY 30

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SENEXON-S 
docusate sodium -sennosides tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55154-6816(NDC:0536-4086)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
docusate sodium (UNII: F05Q2T2JA0) (docusate - UNII:M7P27195AG) docusate sodium50 mg
sennosides a and b (UNII: 1B5FPI42EN) (sennosides a and b - UNII:1B5FPI42EN) sennosides a and b8.6 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX (UNII: R12CBM0EIZ)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColororangeScoreno score
ShapeROUNDSize9mm
FlavorImprint Code TCL081
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55154-6816-930 in 1 BLISTER PACK; Type 0: Not a Combination Product03/16/201112/15/2015
2NDC:55154-6816-328 in 1 BLISTER PACK; Type 0: Not a Combination Product03/16/201111/15/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33403/16/201112/15/2015
Labeler - Cardinal Health (188557102)
Registrant - TIME-CAP LABS, INC (037052099)
Establishment
NameAddressID/FEIBusiness Operations
Cardinal Health188557102REPACK(55154-6816)

Revised: 9/2017
 
Cardinal Health