SENNA SYRUP

Manufacturer
ATLANTIC BIOLOGICALS CORP.
Effective date
2019-05-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:59:31

Label at a glance#

ProductSENNA
Active ingredientSENNOSIDES A AND B
Label structure9 sections

Indications and uses

relieves occasional constipation (irregularity) generally causes bowel movement in 6 to 12 hours

Dosage and administration

shake well before use take preferably at bedtime or as directed by a doctor

Storage and handling

Store at room temperature 15°-30°C (59°-86°F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each 5 ml) purpose
Sennosides 8.8 mg …………………………................Laxative

Uses

OTC - PURPOSE SECTION

relieves occasional constipation (irregularity)
generally causes bowel movement in 6 to 12 hours

Directions

INDICATIONS & USAGE SECTION

shake well before use
take preferably at bedtime or as directed by a doctor

DOSAGE & ADMINISTRATION SECTION

Age                                                                   Starting Dose                           Maximum Dose
adults and children                                   12 years 2 - 3 teaspoonfuls         3 teaspoonfuls twice a day
and older once a day


6 years to under 12 years of age              1 - 1½ teaspoonfuls once a day       1½ teaspoonfuls twice a day

2 to under 6 years of age                       ½ - ¾ teaspoon once a day                 ¾ teaspoon once a day

under 2 years of age consult a doctor consult a doctor

Warnings

WARNINGS SECTION

Do Not Use • laxative products for longer than 1 week
unless directed by a doctor
Ask a doctor or pharmacist before use if you have
• stomach pain • nausea • vomiting
• notice a sudden change in bowel movement that continues
over a period of 2 weeks
Stop use and ask a doctor if
you have rectal bleeding or failure to have a bowel movement
after use of laxative. These may indicate a serious condition
If pregnant or breast-feeding, ask a health
professional before use

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Flavors, parabens, propylene gylcol, sucrose and water

STORAGE AND HANDLING SECTION

Store at room temperature 15°-30°C (59°-86°F)

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN SECTION
In case of accidental
overdose, get medical help or contact a Poison Control Center
immediately

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image 1image 1

image 2image 2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
702311sennosides 8.8 MG in 5 mL Oral SolutionPSN2
702311sennosides, USP 1.76 MG/ML Oral SolutionSCD2
702311sennosides 8.8 MG per 5 mL Oral SyrupSY2
702311sennosides, USP 26.4 MG per 15 ML Oral SolutionSY2
702311sennosides, USP 8.8 MG per 5 ML Oral SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17856-1107-12021-01-29C16284748780-1ba0f9c33-30b4-a910-e053-dadaa90a0b85SENNA SYRUP
17856-1107-22021-01-29C16284748780-1ba0f9c33-30b4-a910-e053-dadaa90a0b85SENNA SYRUP
17856-1107-32021-01-29C16284748780-1ba0f9c33-30b4-a910-e053-dadaa90a0b85SENNA SYRUP
17856-1107-52021-01-29C16284748780-1ba0f9c33-30b4-a910-e053-dadaa90a0b85SENNA SYRUP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-1107-1SENNA10 mL in 1 CUP, UNIT-DOSELIQUID102
17856-1107-2SENNA2.5 mL in 1 SYRINGELIQUID2.52
17856-1107-2SENNA120 in 1 BOX, UNIT-DOSELIQUID1202
17856-1107-3SENNA48 in 1 BOX, UNIT-DOSELIQUID482
17856-1107-3SENNA5 mL in 1 SYRINGELIQUID52
17856-1107-5SENNA5 mL in 1 CUP, UNIT-DOSELIQUID52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-1107SENNA (SENNOSIDES A AND B) LIQUID [ATLANTIC BIOLOGICALS CORP.]2Legacy NDC, 6 package rows20190524_9ad6c4ef-6ae6-4228-a625-02d5548da486.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
54162-007-08ML - Milliliter54162-00766d9c4d9-e409-4a4b-bc98-cbcb59494c0112013-02-13

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17856-110717856-1107-1, 17856-1107-5, 17856-1107-2, 17856-1107-3
54162-007

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
64417ad8-dd57-4c58-973c-97416ec4219a9ad6c4ef-6ae6-4228-a625-02d5548da4862019-05-23WarningsExact identifier
spl id: 64417ad8-dd57-4c58-973c-97416ec4219a
spl set id: 9ad6c4ef-6ae6-4228-a625-02d5548da486

Reported adverse events (FAERS/openFDA)#

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