Docusate Sodium Liquid

Product NDC: 54859-813
11-digit product format: 548590813
Labeler code: 54859
Product ID: 54859-813_4745fe35-8aba-b427-e063-6394a90ab073
Type: HUMAN OTC DRUG
Nonproprietary name: Docusate Sodium
Dosage form: LIQUID
Route: ORAL
Labeler: LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-12-01
Substance: DOCUSATE SODIUM
Active strength: 50 mg/5mL
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: Docusate Sodium Liquid
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DOCUSATE SODIUM	50 mg/5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
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
1248119	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
2d8bdd3e-f6e6-43f5-b3b0-e5a882cae41c	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
54859-813-16	Docusate Sodium Liquid	473 mL in 1 BOTTLE	LIQUID	473		9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
54859-813-16	ML - Milliliter	54859-813	25502fa9-6f5b-4d15-898f-034a45e4599b	1	2025-05-14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
54859-813	DOCUSATE SODIUM LIQUID (DOCUSATE SODIUM) LIQUID [LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION]	8	Current NDC, Legacy NDC, 1 package rows	20241228_2d8bdd3e-f6e6-43f5-b3b0-e5a882cae41c.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 20 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
up and up fiber therapy	PSYLLIUM HUSK	Target Corporation	674753ee-1174-4c06-9ed3-a090b338a39e	2025-11-05	Warnings	Exact identifier application number: M007
up and up fiber therapy	PSYLLIUM HUSK	TARGET CORPORATION	956c48f8-c705-4a86-9866-c68a48ddeb6c	2025-11-05	Warnings	Exact identifier application number: M007
CEO-TWO	LAXATIVE	Beutlich Pharmaceuticals, LLC	08670636-5795-4db0-e063-6294a90afa4b	2025-11-05	Warnings	Exact identifier application number: M007
up and up gentle laxative	BISACODYL	Target Corporation	4a29dc2b-b68f-471b-a84e-4a5096aa3748	2025-11-04	Warnings	Exact identifier application number: M007
Target Fiber Laxative	PSYLLIUM HUSK	TARGET CORPORATION	a581116a-392d-4ac3-ae15-4318506a7b2a	2025-11-04	Warnings	Exact identifier application number: M007
up and up fiber therapy	CALCIUM POLYCARBOPHIL	Target Corporation.	e5473950-06f4-4ea4-975b-3ac94957e776	2025-11-04	Warnings	Exact identifier application number: M007
up and up fiber therapy Natural Fiber	PSYLLIUM HUSK	Target Corporation	f8b1c831-6fd0-4a58-9726-4e0f986c8084	2025-11-04	Warnings	Exact identifier application number: M007
OneLAX	BISACODYL	AKRON PHARMA INC	be4eeb4d-df29-45dc-94ff-933e52c8b6f6	2025-11-03	Warnings	Exact identifier application number: M007
Gentle Stool Softener	DOCUSATE SODIUM	WALGREEN COMPANY	169b33f9-e559-47bf-bbba-c7eda4762c7f	2025-10-31	Warnings	Exact identifier application number: M007
Senna S	DOCUSATE SODIUM, SENNOSIDES	Walgreens	765bfd9b-7a21-4315-9add-cf13007722d5	2025-10-31	Warnings	Exact identifier application number: M007
Gentle Stool Softener	DOCUSATE SODIUM	WALGREEN COMPANY	71b15339-2585-4fae-8445-6fbb4f0a378e	2025-10-31	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Major Pharmaceuticals	97561cd4-63d9-44c2-a3a3-ec668a09a4ed	2025-10-31	Warnings	Exact identifier application number: M007
Fiber Caplets	CALCIUM POLYCARBOPHIL	SAFEWAY	08e2e8b0-90b3-48d6-a72a-40688c74771a	2025-10-29	Warnings	Exact identifier application number: M007
Glycerin	GLYCERIN	Chain Drug Marketing Association Inc.	424d91f0-ecf9-6d9b-e063-6394a90a8006	2025-10-29	Warnings	Exact identifier application number: M007
Publix Laxative Maximum Strength	CALCIUM SENNOSIDES	PUBLIX SUPER MARKETS, INC	11112859-ef1e-4b37-9915-ba4d06a3f198	2025-10-28	Warnings	Exact identifier application number: M007
Publix Stimulant Laxative	BISACODYL	PUBLIX SUPER MARKETS, INC	02e596a7-b8e5-4f55-9bc6-6d17e0fabda7	2025-10-28	Warnings	Exact identifier application number: M007
PUBLIX	PSYLLIUM HUSK	PUBLIX SUPER MARKETS, INC	55f98d3f-f282-4f19-b373-0b59640d274d	2025-10-28	Warnings	Exact identifier application number: M007
PUBLIX	CALCIUM POLYCARBOPHIL	PUBLIX SUPER MARKETS, INC	02e3f4ce-8961-425c-98a9-3b9d66709ca5	2025-10-28	Warnings	Exact identifier application number: M007
Publix Women Laxative	BISACODYL	PUBLIX SUPER MARKETS, INC	03eeca55-f239-4a01-a900-c1943f27a834	2025-10-28	Warnings	Exact identifier application number: M007
Publix Fiber Therapy Orange Smooth	PSYLLIUM HUSK	PUBLIX SUPER MARKETS, INC	b9c54c20-cd82-4627-9217-a66834db4799	2025-10-28	Warnings	Exact identifier application number: M007

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1248119	docusate sodium 50 MG in 5 mL Oral Suspension	PSN	2d8bdd3e-f6e6-43f5-b3b0-e5a882cae41c	9
1248119	docusate sodium 10 MG/ML Oral Suspension	SCD	2d8bdd3e-f6e6-43f5-b3b0-e5a882cae41c	9
1248119	docusate sodium 100 MG per 10 ML Oral Suspension	SY	2d8bdd3e-f6e6-43f5-b3b0-e5a882cae41c	9
1248119	docusate sodium 150 MG per 15 ML Oral Suspension	SY	2d8bdd3e-f6e6-43f5-b3b0-e5a882cae41c	9
1248119	docusate sodium 50 MG per 5 ML Oral Suspension	SY	2d8bdd3e-f6e6-43f5-b3b0-e5a882cae41c	9
1248119	DOSS Sodium 10 MG/ML Oral Suspension	SY	2d8bdd3e-f6e6-43f5-b3b0-e5a882cae41c	9
1248119	docusate sodium 50 MG in 5 mL Oral Suspension	PSN	efe4bf81-fb99-4755-aa23-4f8df5973be8	3
1248119	docusate sodium 10 MG/ML Oral Suspension	SCD	efe4bf81-fb99-4755-aa23-4f8df5973be8	3
1248119	docusate sodium 100 MG per 10 ML Oral Suspension	SY	efe4bf81-fb99-4755-aa23-4f8df5973be8	3
1248119	docusate sodium 150 MG per 15 ML Oral Suspension	SY	efe4bf81-fb99-4755-aa23-4f8df5973be8	3
1248119	docusate sodium 50 MG per 5 ML Oral Suspension	SY	efe4bf81-fb99-4755-aa23-4f8df5973be8	3
1248119	DOSS Sodium 10 MG/ML Oral Suspension	SY	efe4bf81-fb99-4755-aa23-4f8df5973be8	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
54859-813-16	54859081316	473 mL in 1 BOTTLE (54859-813-16)	473 ml	2021-12-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Llorens-Ducosate Sodium 813	LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION	2025-12-31	HUMAN OTC DRUG LABEL	9
SAFECOR HEALTH Docusate Sodium Liquid Drug Facts	Safecor Health, LLC	2025-01-08	HUMAN OTC DRUG LABEL	3