FDA.reportPublic FDA data

Sennosides

Manufacturer
Bryant Ranch Prepack
Effective date
2025-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:07:19

Label at a glance#

ProductSennosides
Active ingredientSENNOSIDES
Label structure11 sections

Indications and uses

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

Dosage and administration

 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 once a day 4 tablets twice a day children 6 to under 12 years 1 tablet once a day 2 tablets twice a day children 2 to under 6 years 1/2 tablet once a day 1 tablet twice a day children under 2 years ask a doctor ask a doctor

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each tablet)
Sennosides 8.6 mg

OTC - PURPOSE SECTION

Purpose
Laxative

Uses

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

OTC - DO NOT USE SECTION

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

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

 stomach pain

 nausea

 vomiting

 noticed a sudden change in bowel habits that continues over a period of 2 weeks

OTC - STOP USE SECTION

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.

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.

OVERDOSAGE SECTION

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

 take preferably at bedtime or as directed by a doctor

agestarting dosagemaximum dosage
adults and children 12
years of age and over 		2 tablets once
a day 		4 tablets twice
a day
children 6 to under
12 years 		1 tablet once
a day 		2 tablets twice
a day
children 2 to under
6 years 		1/2 tablet once
a day 		1 tablet twice
a day
children under
2 years 		ask a doctorask a doctor

Other information

OTHER SAFETY INFORMATION

each tablet contains: calcium 20 mg.
 store in a dry place at 15° – 30°C (59° – 86°F).

INACTIVE INGREDIENT SECTION

croscarmellose sodium, dicalcium phosphate, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, mineral oil, polyethylene glycol, talc.

Questions or comments?

OTC - QUESTIONS SECTION

1-800-616-2471

SPL UNCLASSIFIED SECTION

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

Distributed by:
MAJOR® PHARMACEUTICALS
Indianapolis, IN 46268


*This product is not manufactured or distributed by Avrio Health L.P., owner of the registered trademark Senokot®.

HOW SUPPLIED

How Supplied Section

Sennosides 8.6 mg: color brown, round shape and the imprint code W2.

NDC: 71335-2660-1: 100 Tablets in a BOTTLE

NDC: 71335-2660-2: 60 Tablets in a BOTTLE

NDC: 71335-2660-3: 120 Tablets in a BOTTLE

NDC: 71335-2660-4: 56 Tablets in a BOTTLE

NDC: 71335-2660-5: 30 Tablets in a BOTTLE

NDC: 71335-2660-6: 90 Tablets in a BOTTLE

NDC: 71335-2660-7: 10 Tablets in a BOTTLE

Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sennosides 8.6mg Tablet

Label
Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312935sennosides 8.6 MG Oral TabletPSN1
312935sennosides, USP 8.6 MG Oral TabletSCD1
312935sennosides A and B 8.6 MG Oral TabletSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-2660-1Sennosides100 in 1 BOTTLETABLET, FILM COATED1001
71335-2660-2Sennosides60 in 1 BOTTLETABLET, FILM COATED601
71335-2660-3Sennosides120 in 1 BOTTLETABLET, FILM COATED1201
71335-2660-4Sennosides56 in 1 BOTTLETABLET, FILM COATED561
71335-2660-5Sennosides30 in 1 BOTTLETABLET, FILM COATED301
71335-2660-6Sennosides90 in 1 BOTTLETABLET, FILM COATED901
71335-2660-7Sennosides10 in 1 BOTTLETABLET, FILM COATED101

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0904-7252-60EA - Each0904-72528b411302-6cf8-4c67-887c-46174dec28f112023-03-13
0904-7252-61EA - Each0904-72524c7910a9-1558-4a7a-b204-d7064779beea12023-04-07
0904-7252-80EA - Each0904-725270b43092-f10c-4350-9488-9b7bae9b8d2512023-03-13

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71335-266071335-2660-1, 71335-2660-2, 71335-2660-3, 71335-2660-4, 71335-2660-5, 71335-2660-6, 71335-2660-7
0904-7252

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
NameUNIIKind
DIBASIC CALCIUM PHOSPHATE DIHYDRATEO7TSZ97GEPIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
TALC7SEV7J4R1UIACT
MALTODEXTRIN7CVR7L4A2DIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
LIGHT MINERAL OILN6K5787QVPIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT
SENNOSIDES3FYP5M0IJXACTIB
MAGNESIUM STEARATE70097M6I30IACT
CROSCARMELLOSE SODIUMM28OL1HH48IACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SennosidesSENNOSIDESBryant Ranch Prepackd4ab04e4-b78a-4afc-aa16-d9dc8fb6cc102025-07-14WarningsExact identifier
ndc (package): 71335-2660-3
ndc (package): 71335-2660-7
ndc (package): 71335-2660-6
ndc (package): 71335-2660-2
ndc (package): 71335-2660-4
ndc (package): 71335-2660-5
ndc (package): 71335-2660-1
ndc (product): 71335-2660
ndc11 (package): 71335266004
ndc11 (package): 71335266001
ndc11 (package): 71335266006
ndc11 (package): 71335266003
ndc11 (package): 71335266005
ndc11 (package): 71335266002
ndc11 (package): 71335266007
spl id: 644bf13d-7b0c-4042-b8a2-d017af5ab911
spl set id: d4ab04e4-b78a-4afc-aa16-d9dc8fb6cc10
SennosidesSENNOSIDESMajor Pharmaceuticalsdf3b431b-a1ad-91dd-e053-2995a90aa02f2024-12-06WarningsExact identifier
ndc (product): 0904-7252

Reported adverse events (FAERS/openFDA)#

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