Senna-Lax

Manufacturer
Guardian Drug Company
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:47:55

Label at a glance#

ProductSenna-Lax
Active ingredientSENNOSIDES
Label structure9 sections

Indications and uses

relieves: occasional constipation (irregularity)

Dosage and administration

take preferably at bedtime expect results in 6-12 hours adults and children 12 years and over do not exceed 8 tablets in 24 hours children 6 to under 12 years do not exceed 4 tablets in 24 hours children 2 to under 6 years do not exceed 2 tablets in 24 hours do not exceed the maximum dosage of this product  adults and children 12 years and over 2 tablets once daily (maximum: 4 tablets twice a day)   children 6 to ...

Storage and handling

do not use if printed seal under cap is torn or missing store at room temperature avoid excessive humidity

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Sennosides 8.6 mg

Purpose

OTC - PURPOSE SECTION

Laxative

Uses

INDICATIONS & USAGE SECTION

relieves: occasional constipation (irregularity)

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

  • laxative products for longer than 1 week unless directed by a doctor
Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • abdominal 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, ask a health professional before use 

OTC - PREGNANCY OR BREAST FEEDING SECTION

keep out of reach of children. In case of overdose, get medical help or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • take preferably at bedtime
  • expect results in 6-12 hours
  • adults and children 12 years and over do not exceed 8 tablets in 24 hours
  • children 6 to under 12 years do not exceed 4 tablets in 24 hours
  • children 2 to under 6 years do not exceed 2 tablets in 24 hours
  • do not exceed the maximum dosage of this product
 adults and children 12 years and over2 tablets once daily (maximum: 4 tablets twice a day) 
 children 6 to under 12 years 1 tablet once daily (maximum: 2 tablets twice a day)
 children 2 to under 6 years 1/2 tablet once daily (maximum: 1 tablet twice a day)
 childrem under 2 years ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • do not use if printed seal under cap is torn or missing
  • store at room temperature
  • avoid excessive humidity

Inactive ingredients

INACTIVE INGREDIENT SECTION

crospovidone, dextrose, magnesium stearate, microcrystalline cellulose, pregelatinized starch

PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to the active ingredient in SENOKOT®

Senna-Lax

Natural Vegetable Laxative

Sennosides / Laxative

For Gentle, Overnight

Relief of Constipation

100 Tablets

BoxBox

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312935sennosides 8.6 MG Oral TabletPSN4
312935sennosides, USP 8.6 MG Oral TabletSCD4
312935sennosides A and B 8.6 MG Oral TabletSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53041-159-14Senna-Lax1 in 1 CARTONTABLET14
53041-159-14Senna-Lax50 in 1 BOTTLETABLET504
53041-159-16Senna-Lax1 in 1 CARTONTABLET14
53041-159-16Senna-Lax100 in 1 BOTTLETABLET1004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53041-159SENNA-LAX (SENNOSIDES) TABLET [GUARDIAN DRUG COMPANY]4Current NDC, Legacy NDC, 4 package rows20241222_d3ee7288-986e-44a6-8aa2-05405210c875.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SENNOSIDESACTIVE INGREDIENT3FYP5M0IJX1
SENNOSIDESACTIVE MOIETY3FYP5M0IJX1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61U1
CROSPOVIDONEINACTIVE INGREDIENT68401960MK1
DEXTROSEINACTIVE INGREDIENTIY9XDZ35W21
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I301
STARCH, PREGELATINIZED CORNINACTIVE INGREDIENTO8232NY3SJ1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53041-15953041-159-14, 53041-159-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 12 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
STARCH, PREGELATINIZED CORNSTARCH, CORNO8232NY3SJTABLET / ORAL1116 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
DEXTROSEDEXTROSEIY9XDZ35W2TABLET / ORAL183.66 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
DEXTROSEDEXTROSEIY9XDZ35W2TABLET / ORAL183.66 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
STARCH, PREGELATINIZED CORNSTARCH, CORNO8232NY3SJTABLET / ORAL1116 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
DEXTROSEDEXTROSEIY9XDZ35W2TABLET / ORAL183.66 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
STARCH, PREGELATINIZED CORNSTARCH, CORNO8232NY3SJTABLET / ORAL1116 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET / ORAL980 mgExact identifier — unii+route+dosage form
3 equally ranked IID candidates

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-LaxSENNOSIDESGuardian Drug Companyd3ee7288-986e-44a6-8aa2-05405210c8752024-12-19WarningsExact identifier
ndc (package): 53041-159-14
ndc (package): 53041-159-16
ndc (product): 53041-159
ndc11 (package): 53041015916
ndc11 (package): 53041015914
spl id: dd385d1a-6a28-46fa-bebe-447985c71135
spl set id: d3ee7288-986e-44a6-8aa2-05405210c875

Reported adverse events (FAERS/openFDA)#

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