SENNA-PLUS

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: SENNA-PLUS
Generic name: SENNOSIDES AND DOCUSATE SODIUM
Manufacturer: Geri-Care Pharmaceutical Corp
Product type: HUMAN OTC DRUG
SPL set ID: 8a0882ed-f623-2359-e053-2995a90a6f98
SPL ID: 27ff1c70-104a-4f88-e063-6394a90a7e82
Version: 6
Effective date: 2024-11-28
Source export date: 2026-11-06
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:46:17

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		SENNA-PLUS	openfda.brand_name
generic name		SENNOSIDES AND DOCUSATE SODIUM	openfda.generic_name
manufacturer name		Geri-Care Pharmaceutical Corp	openfda.manufacturer_name
ndc	package	57896-555-20	openfda.package_ndc
ndc	package	57896-555-10	openfda.package_ndc
ndc	package	57896-555-01	openfda.package_ndc
ndc	package	57896-555-06	openfda.package_ndc
ndc	product	57896-555	openfda.product_ndc
ndc11	package	57896055510	derived:openfda.package_ndc
ndc11	package	57896055501	derived:openfda.package_ndc
ndc11	package	57896055520	derived:openfda.package_ndc
ndc11	package	57896055506	derived:openfda.package_ndc
rxcui		998740	openfda.rxcui
spl id		27ff1c70-104a-4f88-e063-6394a90a7e82	id
spl set id		8a0882ed-f623-2359-e053-2995a90a6f98	set_id
unii		3FYP5M0IJX	openfda.unii
unii		F05Q2T2JA0	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings 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 or vomiting have noticed a sudden change in bowel habits that lasts over two 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. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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