Drug Mart Vegetable Laxative plus Stool Softener

Manufacturer
Discount Drug Mart, Inc | Strive Pharmaceuticals Inc.
Effective date
2024-12-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:49:35

Label at a glance#

ProductDrug Mart Vegetable Laxative plus Stool Softener
Active ingredientDOCUSATE SODIUM, SENNOSIDES
Label structure10 sections

Indications and uses

relieves occasional constipation (irregularity) generally, produces bowel movement in 6 to 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 ½ 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 20 mg, sodium 3 mg (very low sodium) store between 20-25°C (68-77°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 bowel movement in 6 to 12 hours

Warnings

WARNINGS 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

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

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.

If pregnant or breast-feeding, 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • take preferably at bedtime or as directed by a doctor
AgeStarting DosageMaximum Dosage
adults and children

12 years and over

2 tablets once a day4 tablets twice a day
children 6 to

under 12 years

1 tablet once a day2 tablets twice a day
children 2 to

under 6 years

½ tablet once a day1 tablet twice a day
children under

2 years

ask a doctorask a doctor

Other information

STORAGE AND HANDLING SECTION

  • each tablet contains: calcium 20 mg, sodium 3 mg (very low sodium)
  • store between 20-25°C (68-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

croscarmellose sodium, dibasic calcium phosphate, FD&C yellow#6 aluminum lake, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, silicon dioxide, talc, titanium dioxide

Questions?

OTC - QUESTIONS SECTION

1-888-577-8033 Monday-Friday 8am-4pm EST

SPL UNCLASSIFIED SECTION

*COMPARE TO THE ACTIVE INGREDIENTS IN SENOKOT-S®

Gentle Relief of Constipation

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

READ AND KEEP OUTER CARTON FOR COMPLETE PRODUCT INFORMATION

SATISFACTION GUARANTEED
IF DISSATISFIED, RETURN UNUSED PORTION AND PACKAGE TO STORE WHERE PURCHASED. IF UNABLE TO RETURN TO STORE, SEND REASON FOR DISSATISFACTION, NAME, ADDRESS AND EMPTY PACKAGE TO: DISCOUNT DRUG MART,211 COMMERCE DRIVE, MEDINA, OHIO 44256

DISTRIBUTED BY:
DRUG MART-FOOD FAIR
MEDINA, OHIO 44256
WWW.DISCOUNT-DRUGMART.COM

Product of India
Packaged and Quality Assured in the USA

* This product is not manufactured or distributed by Purdue Products L.P., distributor of Senokot-S®.

Dual Action
Natural Vegetable Laxative Plus Stool Softener Gentle, overnight relief of constipation

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lax153Lax153

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
594e2c86-3079-4e6e-96c9-48f7a8afc78dProduct name120230718

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53943-153-01Drug Mart Vegetable Laxative plus Stool Softener100 in 1 BOTTLETABLET1003
53943-153-01Drug Mart Vegetable Laxative plus Stool Softener1 in 1 CARTONTABLET13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53943-153DRUG MART VEGETABLE LAXATIVE PLUS STOOL SOFTENER (DOCUSATE SODIUM, SENNOSIDES) TABLET [DISCOUNT DRUG MART, INC]3Current NDC, Legacy NDC, 2 package rows20250101_1b6d59e8-112f-447f-b6e9-526b7d3bd01e.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53943-15353943-153-01

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Drug Mart Vegetable Laxative plus Stool SoftenerDOCUSATE SODIUM, SENNOSIDESDiscount Drug Mart, Inc1b6d59e8-112f-447f-b6e9-526b7d3bd01e2024-12-13WarningsExact identifier
ndc (package): 53943-153-01
ndc (product): 53943-153
ndc11 (package): 53943015301
spl id: ad393496-9ee6-45f4-8963-dfafc4fe9a23
spl set id: 1b6d59e8-112f-447f-b6e9-526b7d3bd01e

Reported adverse events (FAERS/openFDA)#

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