Stool Softener and Stimulant Laxative

Manufacturer: H-E-B | TIME CAP LABORATORIES, INC.
Effective date: 2025-02-14
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 01:29:00

Label at a glance#

ProductStool Softener and Stimulant Laxative

Active ingredientDOCUSATE SODIUM, SENNOSIDES

Label structure10 sections

Indications and uses

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

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact1-877-290-4008

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients (in each tablet)

Docusate sodium 50 mg

Sennosides 8.6 mg

OTC - PURPOSE SECTION

Purposes

Stool Softener

Stimulant laxative

USES

INDICATIONS & USAGE SECTION

Uses

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

WARNINGS SECTION

Warnings

OTC - DO NOT USE SECTION

Do not use

laxative products for longer than 1 week unless told to do so by a doctor
if you are presently taking mineral oil unless told to do so 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 lasts over 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 could be signs of a serious condition.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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 (1-800-222-1222).

DOSAGE & ADMINISTRATION SECTION

Directions

take only by mouth. Doses may be taken as a single daily dose, preferably in the evening, or in divided doses.

adults and children 12 years and older	take 2-4 tablets daily
children 6 to under 12 years of age	take 1-2 tablets daily
children 2 to under 6 years of age	take up to 1 tablet daily
children under 2	ask a doctor

OTHER SAFETY INFORMATION

Other information

each tablet contains: calcium 20 mg, sodium 6 mg (VERY LOW SODIUM)
Store at 25°C (77°F) excursions permitted between 15°-30°C (59°-86°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients carnauba wax, colloidal silicon dioxide, croscarmellose sodium, dibasic calcium phosphate dihydrate, FD&C red #40 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, sodium benzoate, stearic acid, titanium dioxide

OTC - QUESTIONS SECTION

Questions or comments call 1-877-290-4008

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

209R-HEB 240ct label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
998740	sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet	PSN	3
998740	docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SCD	3
998740	DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
37808-549-29	2025-12-29	C162847	48780-1	2cef2736-7763-d83d-e063-dadaa90ab31f	HEB 209R Sennosides 8.6mg / Docusate Sodium 50mg 240ct
37808-549-29	2025-01-30	C162847	48780-1	2cef2736-7763-d83d-e063-dadaa90ab31f	HEB 209R Sennosides 8.6mg / Docusate Sodium 50mg 240ct

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
37808-549-29	Stool Softener and Stimulant Laxative	240 in 1 BOTTLE	TABLET	240		3

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

Stool Softener and Stimulant Laxative
Docusate Sodium, Sennosides
SILICON DIOXIDE
HYPROMELLOSES
MAGNESIUM STEARATE
POLYETHYLENE GLYCOL, UNSPECIFIED
CARNAUBA WAX
TITANIUM DIOXIDE
SODIUM BENZOATE
MICROCRYSTALLINE CELLULOSE
CROSCARMELLOSE SODIUM
DIBASIC CALCIUM PHOSPHATE DIHYDRATE
FD&C RED NO. 40 ALUMINUM LAKE
STEARIC ACID
DOCUSATE SODIUM
DOCUSATE
SENNOSIDES

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
37808-549	37808-549-29

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
HYPROMELLOSES	3NXW29V3WO	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
POLYETHYLENE GLYCOL, UNSPECIFIED	3WJQ0SDW1A	IACT
CARNAUBA WAX	R12CBM0EIZ	IACT
TITANIUM DIOXIDE	15FIX9V2JP	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
MICROCRYSTALLINE CELLULOSE	OP1R32D61U	IACT
CROSCARMELLOSE SODIUM	M28OL1HH48	IACT
DIBASIC CALCIUM PHOSPHATE DIHYDRATE	O7TSZ97GEP	IACT
FD&C RED NO. 40 ALUMINUM LAKE	6T47AS764T	IACT
STEARIC ACID	4ELV7Z65AP	IACT
DOCUSATE SODIUM	F05Q2T2JA0	ACTIB
SENNOSIDES	3FYP5M0IJX	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stool Softener and Stimulant Laxative	DOCUSATE SODIUM, SENNOSIDES	H-E-B	c19280c2-f968-b582-e053-2995a90a9bd3	2025-02-14	Warnings	Exact identifier ndc (package): 37808-549-29 ndc (product): 37808-549 ndc11 (package): 37808054929 spl id: 2e1460d5-2838-7eda-e063-6394a90a91d5 spl set id: c19280c2-f968-b582-e053-2995a90a9bd3

Reported adverse events (FAERS/openFDA)#

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