SENOKOT-S- sennosides and docusate sodium tablet 
Purdue Products LP

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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Senokot-S
(standardized senna concentrate and docusate sodium)

Drug Facts

Active ingredients (in each tablet)

Docusate sodium         50 mg

Sennosides                      8.6 mg

Purpose

Stool softener

Laxative

Uses

Warnings

Do not use

Ask a doctor before use if you have

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

age starting dosage maximum 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

Inactive ingredients


Inactive ingredients dicalcium phosphate,D&C Yellow #10 Aluminum Lake, FD&C Yellow #6 Aluminum Lake, lecithin, magnesium stearate ,microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, pregelatinized starch, sodium benzoate, talc, and titanium dioxide

©2012, Purdue Products L.P.

Manufactured for:
Purdue Products L.P.
Stamford, CT 06901-3431

By:
Purdue Pharma
575 Granite Court
Pickering, ON L1W 3W8, Canada

302887-0A

Senokot-S 60 Tablets Carton
NDC: 67618-310-60

302887-0A
SENOKOT-S 
standardized senna concentrate and docusate sodium tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:67618-310
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.6 mg
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM 50 mg
Inactive Ingredients
Ingredient Name Strength
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL (UNII: 532B59J990)  
STARCH, CORN (UNII: O8232NY3SJ)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Color ORANGE Score no score
Shape ROUND Size 10mm
Flavor Imprint Code P
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:67618-310-04 4 in 1 BLISTER PACK
2 NDC:67618-310-01 1 in 1 CARTON
2 10 in 1 BLISTER PACK
3 NDC:67618-310-30 1 in 1 CARTON
3 30 in 1 BOTTLE, PLASTIC
4 NDC:67618-310-60 1 in 1 CARTON
4 60 in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part334 10/01/1974
Labeler - Purdue Products LP (141916531)
Registrant - Purdue Pharma LP (932323652)
Establishment
Name Address ID/FEI Business Operations
Purdue Pharma 250955291 MANUFACTURE(67618-310)

Revised: 9/2013
Document Id: 7ff38123-df25-8403-c30f-0084ea8f78ec
Set id: c24cdc5e-62e0-41a6-8afb-512202a569f4
Version: 3
Effective Time: 20130918
 
Purdue Products LP