SENNOSIDES, DOCUSATE SODIUM tablet, film coated

Sennosides, Docusate Sodium by

Drug Labeling and Warnings

Sennosides, Docusate Sodium by is a Otc medication manufactured, distributed, or labeled by Cardinal Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients (in each tablet)

Docusate sodium 50 mg

Sennosides 8.6 mg

PURPOSE

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. 1-800-222-1222

Directions

• take preferably at bedtime or as directed by a doctor

  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

• each tablet contains: calcium 11 mg
• each tablet contains: sodium 4 mg
• store at 25ºC (77ºF); excursions permitted between15º-30ºC (59º-86ºF)

INACTIVE INGREDIENT

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

SPL UNCLASSIFIED SECTION

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

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

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

DISTRIBUTED BY CARDINAL HEALTH
DUBLIN, OHIO 43017
www.myleader.com 1-800-200-6313

CARDINAL HEALTH, the Cardinal Health LOGO,
LEADER, and the Leader LOGO are trademarks or
registered trademarks of Cardinal Health.

100% Money Back Guarantee
Return to place of purchase if not satisfied.

12958-11-18

PRINCIPAL DISPLAY PANEL

LEADER TH

NDC: 70000-0405-1

Senna Plus

Docusate Sodium, 50 mg | Sennosides, 8.6 mg

Stool Softner | Laxative

Dual Action

Standardized Senna

Concentrate

30 TABLETS

Tablet Image

Actula Size

COMPARE TO

SENOKOT-S®

active ingredients

100% Money Back Guarantee

INGREDIENTS AND APPEARANCE

SENNOSIDES, DOCUSATE SODIUM 
sennosides, docusate sodium tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70000-0405
Route of Administration	ORAL

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
TALC (UNII: 7SEV7J4R1U)
HYPROMELLOSES (UNII: 3NXW29V3WO)
STEARIC ACID (UNII: 4ELV7Z65AP)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MAGNESIUM STEARATE (UNII: 70097M6I30)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
STARCH, CORN (UNII: O8232NY3SJ)
TRIACETIN (UNII: XHX3C3X673)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Product Characteristics
Color	yellow	Score	no score
Shape	ROUND	Size	10mm
Flavor		Imprint Code	CPC;490
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70000-0405-1	1 in 1 CARTON	12/19/2018
1		30 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part334	12/19/2018

Labeler - Cardinal Health (097537435)