SENNA SYRUP Natural Vegitable Lexative

Manufacturer
Akron Pharma Inc.
Effective date
2023-03-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:54:34

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

Avoid accessive heat. 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 dosage
 Mulls and children 12 yeart and older 2-3 teaspoons once a day 3 teaspoons twice a day
 Children 6 years to under 12 yeart 1 -11> teaspoons once a day 11> teaspoons twice a day
 Children 2 yeart to under 6 yeart l> -¾teaspoon once a day ¾ teaspoon twice a day
 Children under 2 years ask a doctor ask a doctor

Warnings

WARNINGS SECTION

ask a doctor betore use rt you have • stomach pain • nausea • vomiting • noticed a sudden change in bowel movements that continues over a period of 2 weeks

Do not use laxative produe1s for longer than 1 week unless directed by a doctor

Other Information

STORAGE AND HANDLING SECTION

  • Avoid accessive heat. Store at room temperature 15°-30°C (59°-86°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Mythylparaben, Propylene Glycol, Propylparaben, Purified Water, Sucrose

KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental overdose, get medical help or contact a Poison Control Center immediately

Questions?

To Report Adverse Drug Event Call 1(877) 225-6999

Manufactured for:

Akron Pharma Inc.,

Fairfield, NJ-07004

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

8OZ8OZ

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
702311sennosides 8.8 MG in 5 mL Oral SolutionPSN3
702311sennosides, USP 1.76 MG/ML Oral SolutionSCD3
702311sennosides 8.8 MG per 5 mL Oral SyrupSY3
702311sennosides, USP 26.4 MG per 15 ML Oral SolutionSY3
702311sennosides, USP 8.8 MG per 5 ML Oral SolutionSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71399-8237-8SENNA237 mL in 1 BOTTLESYRUP2373

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71399-8237SENNA SYRUP [AKRON PHARMA INC.]3Legacy NDC, 1 package rows20230327_9e9c434a-7075-45d4-b7b3-0f83a33cf046.zip

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
71399-823771399-8237-8

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
d24f7b42-94ba-4f56-864b-b423cf1e5efe9e9c434a-7075-45d4-b7b3-0f83a33cf0462023-03-18WarningsExact identifier
spl id: d24f7b42-94ba-4f56-864b-b423cf1e5efe
spl set id: 9e9c434a-7075-45d4-b7b3-0f83a33cf046

Reported adverse events (FAERS/openFDA)#

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