HEALIX SENNA-S

Manufacturer
Brainstorm Industries LLC
Effective date
2026-03-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:51:01

Label at a glance#

ProductHEALIX SENNA-S
Active ingredientSENNOSIDES, DOCUSATE SODIUM
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients (in each tablet)

Docusate Sodium .................. 50 mg

Sennosides ........................... 8.6 mg

OTC - PURPOSE SECTION

Docusate Sodium ........ Stool Softener

Sennosides .......................... Laxative

INDICATIONS & USAGE SECTION

Uses

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

WARNINGS SECTION

WARNINGS

OTC - DO NOT USE SECTION

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.

OTC - ASK DOCTOR SECTION

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

OTC - STOP USE SECTION

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.

PREGNANCY SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

DOSAGE & ADMINISTRATION SECTION

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 SAFETY INFORMATION

Other information

  • each tablet contains: calcium 19.92 mg, sodium 5.61 mg

VERY LOW SODIUM

  • store at 25°C (77°F); excursions permitted between 15°C-30°C (59°-86°F)

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Colloidal Silicon Dioxide, Croscarmellose Sodium, Dicalcium

Phosphate, FD&C Red, Hypromellose, Magnesium Stearate,

Maltodextrin, Microcrystalline Cellulose, Polyethylene Glycol 400,

Stearic Acid, Titanium Dioxide.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel

NDC 87275- 2451-10

Healix Senna+S Dual Action

Natural Vegetable Laxative Ingredient + Stool Softener

100 Tabletsin White Bottle

Sennosides 8.6 mg, Docusate Sodium 50 mg

Principle Display PanelPrinciple Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSN1
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCD1
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87275-2451-1HEALIX SENNA-S100 in 1 BOTTLETABLET1001

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
87275-245187275-2451-1

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
HEALIX SENNA-SSENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MGBrainstorm Industries LLC4cc5388f-1716-5d19-e063-6394a90a5a252026-03-11WarningsExact identifier
ndc (package): 87275-2451-1
ndc (product): 87275-2451
ndc11 (package): 87275245101
spl id: 4cc5388f-1717-5d19-e063-6394a90a5a25
spl set id: 4cc5388f-1716-5d19-e063-6394a90a5a25

Reported adverse events (FAERS/openFDA)#

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