Senna-S

Manufacturer
Ulai Health LLC | Pharbest Pharmaceuticals, Inc.
Effective date
2025-01-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:53:20

Label at a glance#

ProductSenna-S
Active ingredientSENNOSIDES, DOCUSATE SODIUM
Label structure9 sections

Indications and uses

relieves occasional constipation (irregularity) generally produces a bowel movement in 6-12 hours

Dosage and administration

take preferably at bedtime or as directed by a doctor age starting dosage maximum dosage adults and children 12 years 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

Storage and handling

each tablet contains:  calcium 10 mg, sodium 5 mg, Very Low Sodium store at 20-25°C(68-77°F); excursions permitted between 15 o -30 o C (59 o -86 o F)

Label contents#

Full prescribing information#

Active Ingredients (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Sennosides 8.6 mg

Docusate Sodium 50 mg

Purpose

OTC - PURPOSE SECTION

Laxative

Stool Softener

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

  • if you are 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 the 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 (1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

  • take preferably at bedtime or as directed by a doctor

age

starting dosage

maximum dosage

adults and children 12 years 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

STORAGE AND HANDLING SECTION

  • each tablet contains:  calcium 10 mg, sodium 5 mg, Very Low Sodium
  • store at 20-25°C(68-77°F); excursions permitted between 15 o-30 oC (59 o-86 oF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

croscarmellose sodium, D&C Yellow# 10, dicalcium phosphate, FD&C Yellow #6, magnesium stearate, microcrystalline cellulose, polyvinyl alcohol, polyethylene glycol, sodium benzoate, talc, titanium dioxide

Questions?

OTC - QUESTIONS SECTION

(866) 562-2756 (Mon-Fri 8 AM to 4 PM EST)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PHARBEST

NDC 73057-378-11

Manufactured in the USA

*Compare to the active ingredients in Senokot-S ®

SENNA-S

Sennosides 8.6 mg &

Docusate Sodium 50 mg

Natural Vegetable Laxative

Ingredient Plus Stool Softener

1000 TABLETS

Ulai Senna S 1000ct LabelUlai Senna S 1000ct Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSN3
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCD3
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73057-378-07Senna-S60 in 1 BOTTLE, PLASTICTABLET, FILM COATED603
73057-378-08Senna-S100 in 1 BOTTLE, PLASTICTABLET, FILM COATED1003
73057-378-11Senna-S1000 in 1 BOTTLE, PLASTICTABLET, FILM COATED10003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73057-378SENNA-S (SENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MG) TABLET, FILM COATED [ULAI HEALTH LLC]3Current NDC, Legacy NDC, 3 package rows20250122_c0e27b02-8ef2-4239-8f8c-790f7d978dc0.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73057-37873057-378-07, 73057-378-08, 73057-378-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Senna-SSENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MGUlai Health LLCc0e27b02-8ef2-4239-8f8c-790f7d978dc02025-01-12WarningsExact identifier
ndc (package): 73057-378-07
ndc (package): 73057-378-11
ndc (package): 73057-378-08
ndc (product): 73057-378
ndc11 (package): 73057037807
ndc11 (package): 73057037811
ndc11 (package): 73057037808
spl id: 2c270be1-981f-3019-e063-6394a90a098f
spl set id: c0e27b02-8ef2-4239-8f8c-790f7d978dc0

Reported adverse events (FAERS/openFDA)#

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