SENNA

Product NDC: 69618-069
11-digit product format: 696180069
Labeler code: 69618
Product ID: 69618-069_2de53996-629d-7455-e063-6294a90a21e4
Type: HUMAN OTC DRUG
Nonproprietary name: SENNOSIDES
Dosage form: SYRUP
Route: ORAL
Labeler: Reliable 1 Laboratories LLC
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-08-03
Substance: SENNOSIDES
Active strength: 8.8 mg/5mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 18 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	69618-069-58	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	69618-069-58	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	69618-069-58	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	69618-069-58	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	69618-069-58	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	69618-069-58	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	69618-069-58	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	69618-069-58	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	69618-069-58	`1332a3947898…`	`d4bfe170f9cd…`

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: SENNA
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SENNOSIDES	8.8 mg/5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

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

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
702311	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
c8aa7ae9-7d00-db7d-e053-2995a90ae72b	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69618-069-58	2023-01-30	C162847	48780-1	f386c64a-0745-0266-e053-dadaa90a7c1a	Senna Syrup

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69618-069-58	SENNA	237 mL in 1 BOTTLE, PLASTIC	SYRUP	237		4

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
69618-069-58	ML - Milliliter	69618-069	576c7147-81a3-4d0f-8e74-5a33f9b1e2c8	1	2021-09-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69618-069	SENNA (SENNOSIDES) SYRUP [RELIABLE 1 LABORATORIES LLC]	4	Current NDC, Legacy NDC, 1 package rows	20250213_c8aa7ae9-7d00-db7d-e053-2995a90ae72b.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 32 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
NuValu Epsom Salt	MAGNESIUM SULFATE (HEPTAHYDRATE)	J C SALES	5a503d8d-7899-4b1e-be6f-8e2a759af265	2024-12-04	Warnings	Exact identifier application number: M007
SENNOSIDES	SENNOSIDES	CVS Pharmacy, Inc.	6dffc3f5-bae0-c436-e053-2991aa0a0f8b	2024-12-02	Warnings	Exact identifier application number: M007
Pure and Gentle	MINERAL OIL	Medline Industries, LP	96d4cad5-0602-4c31-94ed-3117b4fd4a94	2024-11-26	Warnings	Exact identifier application number: M007
Pure and Gentle Laxative	SODIUM PHOSPHATE	Medline Industries, LP	e3165538-75dd-4f0f-adc8-d4075de10f1e	2024-11-26	Warnings	Exact identifier application number: M007
DOCUSATE SODIUM 50 MG	DOCUSATE SODIUM	Humanwell PuraCap Pharmaceutical (Wuhan), Ltd.	af7533e6-8b06-48a4-940e-7ecb57b24b59	2024-11-25	Warnings	Exact identifier application number: M007
DOCUSATE SODIUM 100mg Two-Tone	DOCUSATE SODIUM	Humanwell PuraCap Pharmaceutical (Wuhan), Ltd.	a923e5ca-86fd-4bf9-9931-180ddfdeae66	2024-11-25	Warnings	Exact identifier application number: M007
DOCUSATE SODIUM 100mg Two-Tone	DOCUSATE SODIUM	Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd.	7cf1df18-d658-4bff-8a62-365fc5656942	2024-11-25	Warnings	Exact identifier application number: M007
DOCUSATE SODIUM 100mg	DOCUSATE SODIUM	Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd.	c5bdfbfc-d24a-4088-9b60-ecea8120ff43	2024-11-25	Warnings	Exact identifier application number: M007
DOCUSATE SODIUM	DOCUSATE SODIUM	Humanwell PuraCap Pharmaceutical (Wuhan), Ltd.	b10fdf50-289e-41f3-9b83-a4e4dd892f88	2024-11-21	Warnings	Exact identifier application number: M007
DOCUSATE SODIUM 100mg Two-Tone	DOCUSATE SODIUM	Humanwell PuraCap Pharmaceutical (Wuhan), Ltd.	85c64624-428d-46fa-8071-f42b8feec049	2024-11-21	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	Humanwell PuraCap Pharmaceuticals (Wuhan) Co., Ltd	33251cb7-b7b1-4f6c-9e10-4fa64cbf03a0	2024-11-21	Warnings	Exact identifier application number: M007
STOOL SOFTENER	DOCUSATE SODIUM	Walgreen Co.	d8d97ca5-5131-4620-8ce9-bc3f9d5c0ab5	2024-11-21	Warnings	Exact identifier application number: M007
4718 Enema, Mineral Oil	4718 ENEMA, MINERAL OIL	Dynarex	9e51c852-9477-5cf5-e053-2a95a90a97db	2024-11-20	Warnings	Exact identifier application number: M007
Relief	SODIUM PHOSPHATE, MONOBASIC AND SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE	Leosons Overseas Corp	5b301d5b-1e2c-47ed-a05f-d6be0fdfc940	2024-11-19	Warnings	Exact identifier application number: M007
REFLIEF SALINE LAXATIVE PEDIATRIC READY TO USE	SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM	Leosons Overseas Corp	90e7c2b4-35e1-4a27-afea-9257c480e190	2024-11-19	Warnings	Exact identifier application number: M007
Stool Softener	DOCUSATE SODIUM 100MG	PuraCap Pharmaceutical LLC	272c86f1-f229-2ebf-e063-6394a90a3471	2024-11-18	Warnings	Exact identifier application number: M007
Milk of Magnesia Concentrate	MAGNESIUM HYDROXIDE	PAI Holdings, LLC dba PAI Pharma	2a99a1a8-a830-429f-9cfd-3f29c3d3547c	2024-11-12	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	A-S Medication Solutions	122486e9-74dd-4181-97d1-0b07688280f4	2024-11-06	Warnings	Exact identifier application number: M007
Stratuscare Adult Glycerin	GLYCERIN	Stratus Pharmaceuticals	3e1935da-5c1f-4942-98dd-320fade82321	2024-11-04	Warnings	Exact identifier application number: M007
DOCUSATE SODIUM	DOCUSATE SODIUM	NuCare Pharmaceuticals,Inc.	fdf3c8e1-d554-4cdb-e053-6394a90a542e	2024-11-01	Warnings	Exact identifier application number: M007

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
3FYP5M0IJX	SENNOSIDES	SENNOSIDES

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
702311	sennosides 8.8 MG in 5 mL Oral Solution	PSN	c8aa7ae9-7d00-db7d-e053-2995a90ae72b	4
702311	sennosides, USP 1.76 MG/ML Oral Solution	SCD	c8aa7ae9-7d00-db7d-e053-2995a90ae72b	4
702311	sennosides 8.8 MG per 5 mL Oral Syrup	SY	c8aa7ae9-7d00-db7d-e053-2995a90ae72b	4
702311	sennosides, USP 26.4 MG per 15 ML Oral Solution	SY	c8aa7ae9-7d00-db7d-e053-2995a90ae72b	4
702311	sennosides, USP 8.8 MG per 5 ML Oral Solution	SY	c8aa7ae9-7d00-db7d-e053-2995a90ae72b	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69618-069-58	69618006958	237 mL in 1 BOTTLE, PLASTIC (69618-069-58)	237 ml	2021-08-03	0000-00-00	No	No	Current