FDA.reportPublic FDA data

Senna Natural Relief

Manufacturer
Pioneer Life Sciences, LLC
Effective date
2025-12-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:29:24

Label at a glance#

ProductSenna Natural Relief
Active ingredientSENNOSIDES
Label structure13 sections

Indications and uses

relieves occasional constipation (irregularity). generally prodcues 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 & 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#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Sennosides 8.6 mg

Purpose

OTC - PURPOSE SECTION

Laxative

Uses:

INDICATIONS & USAGE SECTION

  • relieves occasional constipation (irregularity).
  • generally prodcues a bowel movement in 6-12 hours

Warnings:

WARNINGS SECTION

Do not use

  • 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.

KEEP OUT OF REACH OF CHILDREN

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 Control Center (1-800-222-1222) right away. 

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Take preferably at bedtime or as directed by a doctor.

age

starting dosage

maximum dosage

adults & 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

OTHER INFORMATION

OTHER SAFETY INFORMATION

  • store at 20-25°C (68-77°F) excursions permitted between15°-30°C (59°-86°F)
  • each tablet contains: Calcium 25 mg & sodium 3 mg

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Colloidal silicon dioxide,croscarmellose sodium, Dicalcium phosphate, Hypromellose, liquid paraffin, magnesium stearate, microcrystalline cellulose, Maltodextrin, Purified water, Sodium lauryl sulphate, Stearic Acid.

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

Call 1-732-698-5070 Monday through Friday 9AM–5PM EST 

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Senna Natural Relief Sennosides 8_6mg 600ctSenna Natural Relief Sennosides 8_6mg 600ct

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312935sennosides 8.6 MG Oral TabletPSN4
312935sennosides, USP 8.6 MG Oral TabletSCD4
312935sennosides A and B 8.6 MG Oral TabletSY4

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128X002N8TBKDSenna Natural Relief Sennosides 8_6mg 600ct.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72090-031-602023-10-25C16284748780-1d6a99b39-e015-a426-e053-dadaa90af4c2ac8b602a-e53c-0b44-e053-2a95a90affa8
72090-031-602022-01-28C16284748780-1d6a99b39-e015-a426-e053-dadaa90af4c2ac8b602a-e53c-0b44-e053-2a95a90affa8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72090-031-60Senna Natural Relief600 in 1 BOTTLETABLET6004

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72090-03172090-031-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM LAURYL SULFATE368GB5141JIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
STEARIC ACID D7T3B081197XIACT
PARAFFINI9O0E3H2ZEIACT
SENNOSIDES3FYP5M0IJXACTIB
DIBASIC CALCIUM PHOSPHATE DIHYDRATEO7TSZ97GEPIACT
HYPROMELLOSES3NXW29V3WOIACT
MAGNESIUM STEARATE70097M6I30IACT
MALTODEXTRIN7CVR7L4A2DIACT
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
Senna Natural ReliefSENNA NATURAL RELIEFPioneer Life Sciences, LLCce0938d4-efd1-4efb-8e51-037f7040080e2025-12-29WarningsExact identifier
ndc (product): 72090-031
Senna Natural ReliefSENNA NATURAL RELIEFPioneer Life Sciences, LLCac8b602a-e53c-0b44-e053-2a95a90affa82025-12-29WarningsExact identifier
ndc (package): 72090-031-60
ndc (product): 72090-031
ndc11 (package): 72090003160
spl id: ae68255e-6cc3-4ab6-bee0-373fbffcc1f0
spl set id: ac8b602a-e53c-0b44-e053-2a95a90affa8

Reported adverse events (FAERS/openFDA)#

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