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: 616a896a-d238-7f7c-e053-2a91aa0a0f5b
SPL ID: 44fb4dda-2232-66bd-e063-6294a90ac8da
Version: 6
Effective date: 2025-12-02
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:29

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	57896-458-06	openfda.package_ndc
ndc	package	57896-458-20	openfda.package_ndc
ndc	package	57896-458-10	openfda.package_ndc
ndc	package	57896-458-01	openfda.package_ndc
ndc	product	57896-458	openfda.product_ndc
ndc11	package	57896045810	derived:openfda.package_ndc
ndc11	package	57896045801	derived:openfda.package_ndc
ndc11	package	57896045806	derived:openfda.package_ndc
ndc11	package	57896045820	derived:openfda.package_ndc
rxcui		998740	openfda.rxcui
spl id		44fb4dda-2232-66bd-e063-6294a90ac8da	id
spl set id		616a896a-d238-7f7c-e053-2a91aa0a0f5b	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 for more than 1 week unless directed by a doctor Ask a doctor before use if you have abdominal pain, nausea or vomiting are taking mineral oil have noticed a sudden change in bowel habits that lasts over 2 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.