SENOKOT

Manufacturer: A-S Medication Solutions
Effective date: 2026-09-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: daily-update
Hydrated at: 2026-09-11 03:01:20

Label at a glance#

ProductSENOKOT

Active ingredientSENNOSIDES

Label structure15 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts

Active ingredient (in each tablet)

Sennosides 8.6mg

Purpose

OTC - PURPOSE SECTION

Laxative

INDICATIONS & USAGE SECTION

Uses

relieves occasional constipation (irregularity)
generally produces a bowel movement in 6–12 hours

WARNINGS SECTION

Warnings

OTC - DO NOT USE SECTION

Do not use

laxative products for longer than 1 week unless directed by a doctor

OTC - ASK DOCTOR/PHARMACIST SECTION

Aska doctor before use if you have

stomach pain
nausea
vomiting
noticed a sudden change in bowel habits that continues overa period of 2 weeks

OTC - STOP USE SECTION

Stop use and ask a doctorif you have rectal bleeding or fail to have a bowel movementafter use of a laxative. These may indicate a serious condition.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison ControlCenter right away.

DOSAGE & ADMINISTRATION SECTION

Directions

take preferably at bedtime or as directed by a doctor

age	starting dosage	maximum dosage
adults and children 12 years of age and over	2 tablets oncea day	4 tablets twicea day
children 6 to under12 years	1 tablet once aday	2 tablets twicea day
children 2 to under6 years	1/2 tablet oncea day	1 tablet twicea day
children under2 years	ask a doctor	ask a doctor

SPL UNCLASSIFIED SECTION

Other Information

each tablet contains: calcium 20 mg
store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients

croscarmellose sodium, dicalciumphosphate, hypromellose, magnesium stearate, maltodextrin, microcrystallinecellulose, mineral oil, polyethylene glycol, talc

HOW SUPPLIED

HOW SUPPLIED SECTION

Product: 50090-8045

NDC: 50090-8045-0 50 TABLET in a BOTTLE, PLASTIC / 1 in a CARTON

SPL UNCLASSIFIED SECTION

Avrio Health L.P.

305616-0B

standardized senna concentrate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	Data Matrix	(01)00350090804508(17)991231(10)9987654(21)AA000000	GTIN-14: 00350090804508 GTIN-12: 350090804508 UPC-A: 350090804508 EAN-13: 0350090804508 GTIN storage (14 digits): 00350090804508	lbl500908045.jpg

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
67618-300-10	EA - Each	67618-300	6d995b3f-8f49-4111-9050-f18f3f0be499	1	2012-07-24
67618-300-11	EA - Each	67618-300	550247ea-a7f8-4d6f-9cd9-b442d2c9f6d1	1	2012-07-24
67618-300-20	EA - Each	67618-300	029befb9-b71d-41e1-8118-4fac1a66fc44	1	2012-07-24
67618-300-40	EA - Each	67618-300	147e5b3d-423c-45e9-8222-6f15b35fc06d	1	2013-06-04
67618-300-50	EA - Each	67618-300	e8768eff-fab6-4153-9fa7-44686f5e8f05	1	2012-07-24

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

SENOKOT
standardized senna
SENNOSIDES
CROSCARMELLOSE SODIUM
ANHYDROUS DIBASIC CALCIUM PHOSPHATE
HYPROMELLOSE, UNSPECIFIED
MAGNESIUM STEARATE
MALTODEXTRIN
MICROCRYSTALLINE CELLULOSE
MINERAL OIL
POLYETHYLENE GLYCOL, UNSPECIFIED
TALC

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50090-8045	50090-8045-0
67618-300

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SENNOSIDES	3FYP5M0IJX	ACTIB
CROSCARMELLOSE SODIUM	M28OL1HH48	IACT
ANHYDROUS DIBASIC CALCIUM PHOSPHATE	L11K75P92J	IACT
HYPROMELLOSE, UNSPECIFIED	3NXW29V3WO	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
MALTODEXTRIN	7CVR7L4A2D	IACT
MICROCRYSTALLINE CELLULOSE	OP1R32D61U	IACT
MINERAL OIL	T5L8T28FGP	IACT
POLYETHYLENE GLYCOL, UNSPECIFIED	3WJQ0SDW1A	IACT
TALC	7SEV7J4R1U	IACT

Source Document#

Source XML

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SENOKOT	STANDARDIZED SENNA	A-S Medication Solutions	0c6e6bdd-9f49-4550-b60a-8f58b7c0f090	2026-09-09	Warnings	Exact identifier ndc (package): 50090-8045-0 ndc (product): 50090-8045 ndc11 (package): 50090804500 spl id: 2b150b8a-d170-4a1a-863d-aa58c0ec5fda spl set id: 0c6e6bdd-9f49-4550-b60a-8f58b7c0f090
Senokot	STANDARDIZED SENNA CONCENTRATE	Atlantis Consumer Healthcare, Inc.	c18dd7fa-993b-440b-8cdd-f1551abb99ca	2025-12-29	Warnings	Exact identifier ndc (product): 67618-300

Reported adverse events (FAERS/openFDA)#

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