® Tablets

Label at a glance#

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

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.

ACTIVE INGREDIENT (IN EACH TABLET)

OTC - ACTIVE INGREDIENT SECTION

Docusate Sodium 50 mg

Sennosides 8.6 mg

PURPOSE

OTC - PURPOSE SECTION

Stool softener

Stimulant laxative

USES

INDICATIONS & USAGE SECTION

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

WARNINGS

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

• this product if you are presently 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

OTC - ASK DOCTOR SECTION

• 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

OTC - STOP USE SECTION

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,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

• take preferably at bedtime or as directed by a doctor
• do not exceed maximum dosage

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

STORAGE AND HANDLING SECTION

• each tablet contains: calcium 4 mg, sodium 8 mg
• store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

colloidal silicon dioxide, croscarmellose sodium, D&C Yellow #10 Aluminum Lake, FD&C Yellow #6 Aluminum Lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, stearic acid, titanium dioxide

HOW SUPPLIED

How Supplied Section

Docusate Sodium 50 mg & Sennosides 8.6 mg

• NDC 63629-8908-1: 1000 Tablets in a BOTTLE

Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Docusate Sodium 50 mg & Sennosides 8.6 mg

Stool Softner/Laxative

stool softner plus natural vegetable laxative

DailyMed Billing Units#

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

• Senna-S
• Docusate Sodium 50 mg Sennosides 8.6 mg
• CROSCARMELLOSE SODIUM
• CROSCARMELLOSE
• MAGNESIUM STEARATE
• FD&C YELLOW NO. 6
• C.I. FOOD YELLOW 3 (FREE ACID)
• HYPROMELLOSE 2910 (5 MPA.S)
• MICROCRYSTALLINE CELLULOSE
• STEARIC ACID
• POLYETHYLENE GLYCOL 400
• TITANIUM DIOXIDE
• DOCUSATE SODIUM
• DOCUSATE
• SENNOSIDES
• SILICON DIOXIDE
• D&C YELLOW NO. 10

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.