Stool Softener plus Stimulant Laxative

Product NDC: 79481-0304
Requested package NDC: 79481-0304-1
11-digit product format: 794810304
Labeler code: 79481
Product ID: 79481-0304_3118c301-06ff-fd57-e063-6294a90a916f
Type: HUMAN OTC DRUG
Nonproprietary name: Docusate Sodium and Sennosides
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Meijer, Inc.
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-03-01
Substance: SENNOSIDES; DOCUSATE SODIUM
Active strength: 8.6; 50 mg/1; mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Stool Softener plus Stimulant Laxative
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SENNOSIDES	8.6 mg/1
DOCUSATE SODIUM	50 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3FYP5M0IJX	Internal UNII lookup
F05Q2T2JA0	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
998740	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
261a88d6-87d2-7544-e063-6294a90a2e94	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79481-0304-1	Stool Softener plus Stimulant Laxative	100 in 1 BOTTLE	TABLET, FILM COATED	100		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79481-0304	STOOL SOFTENER PLUS STIMULANT LAXATIVE (DOCUSATE SODIUM AND SENNOSIDES) TABLET, FILM COATED [MEIJER, INC.]	2	Current NDC, 1 package rows	20250326_261a88d6-87d2-7544-e063-6294a90a2e94.zip

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 plus Stimulant Laxative	DOCUSATE SODIUM AND SENNOSIDES	Meijer, Inc.	261a88d6-87d2-7544-e063-6294a90a2e94	2025-03-24	Warnings	Exact identifier ndc (package): 79481-0304-1 ndc (product): 79481-0304 ndc11 (package): 79481030401

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
3FYP5M0IJX	SENNOSIDES		SENNOSIDES
F05Q2T2JA0	DOCUSATE SODIUM	577-11-7	DOCUSATE SODIUM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
998740	sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet	PSN	261a88d6-87d2-7544-e063-6294a90a2e94	2
998740	docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SCD	261a88d6-87d2-7544-e063-6294a90a2e94	2
998740	DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SY	261a88d6-87d2-7544-e063-6294a90a2e94	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Sample	Exclude flag	Status
79481-0304-1	79481030401	100 TABLET, FILM COATED in 1 BOTTLE (79481-0304-1)	2025-03-01	No	No	Current