Senexon-S

Manufacturer
RUGBY LABORATORIES | Pharbest Pharmaceuticals, Inc.
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:47:21

Label at a glance#

ProductSenexon-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 15-30 o C (59-86 o F)

Label contents#

Full prescribing information#

Active Ingredients (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Docusate Sodium 50 mg

Sennosides 8.6 mg

Purpose

OTC - PURPOSE SECTION

Stool Softener

Laxative

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 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

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 15-30oC (59-86oF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions or comments?

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RUGBY

NDC 0536-1247-10

Compare to the active ingredients in Senokot-S®*

Senexon-S

Docusate Sodium, 50 mg

Sennosides, 8.6 mg

Natural Vegetable

Laxative Ingredient

+ Stool Softener

1000 TABLETS

Rugby Senexon-S 1000 ct. Product LabelRugby Senexon-S 1000 ct. Product Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1248013Senexon-S 50 MG / 8.6 MG Oral TabletPSN3
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSN3
1248013docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [Senexon S]SBD3
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCD3
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSY3
1248013DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [Senexon S]SY3
1248013Senexon-S (docusate sodium 50 MG / sennosides, USP 8.6 MG) Oral TabletSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0536-1247-01Senexon-S100 in 1 BOTTLE, PLASTICTABLET, FILM COATED1003
0536-1247-10Senexon-S1000 in 1 BOTTLE, PLASTICTABLET, FILM COATED10003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0536-1247SENEXON-S (DOCUSATE SODIUM 50MG AND SENNOSIDES 8.6MG) TABLET, FILM COATED [RUGBY LABORATORIES]3Current NDC, Legacy NDC, 2 package rows20241222_2e758ff1-3083-4245-8f58-1c47b042bfdd.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0536-1247-01EA - Each0536-1247d7ebf6c0-94d1-4058-a337-8a1c4cdc054c12019-11-12
0536-1247-10EA - Each0536-1247fc120350-f269-411f-a810-65f8d76772f012019-11-12

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
0536-12470536-1247-01, 0536-1247-10

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
Senexon-SDOCUSATE SODIUM 50MG AND SENNOSIDES 8.6MGRUGBY LABORATORIES2e758ff1-3083-4245-8f58-1c47b042bfdd2024-12-19WarningsExact identifier
ndc (package): 0536-1247-01
ndc (package): 0536-1247-10
ndc (product): 0536-1247
ndc11 (package): 00536124710
ndc11 (package): 00536124701
spl id: 8ff24a4d-d516-4b17-a838-2a61f19686c5
spl set id: 2e758ff1-3083-4245-8f58-1c47b042bfdd

Reported adverse events (FAERS/openFDA)#

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