SENNA NATURAL RELIEF- senna natural relief tablet 
Pioneer Life Sciences, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredient

Sennosides 8.6 mg

Purpose

Laxative

Uses:

Warnings:

Do not use

Ask a doctor before use if you have

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.

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

KEEP OUT OF REACH OF CHILDREN

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

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

INACTIVE INGREDIENTS

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?

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

PRINCIPAL DISPLAY PANEL

Senna Natural Relief Sennosides 8_6mg 600ct

SENNA NATURAL RELIEF 
senna natural relief tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72090-031
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES8.6 mg
Inactive Ingredients
Ingredient NameStrength
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STEARIC ACID D7 (UNII: T3B081197X)  
PARAFFIN (UNII: I9O0E3H2ZE)  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
Product Characteristics
ColorbrownScoreno score
ShapeROUNDSize10mm
FlavorImprint Code none
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72090-031-60600 in 1 BOTTLE; Type 0: Not a Combination Product08/03/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33408/03/2020
Labeler - Pioneer Life Sciences, LLC (014092742)

Revised: 10/2023
Document Id: dfa82c65-f6db-4911-9e87-37e3472f1bfa
Set id: ac8b602a-e53c-0b44-e053-2a95a90affa8
Version: 2
Effective Time: 20231003
 
Pioneer Life Sciences, LLC