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.

----------

Active Ingredient

Sennosides 8.6 mg

Purpose

Laxative

Uses:

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

Warnings:

Do not use -

Laxative products for longer than 1 week, unless directed by a doctor.

If you have ever had an allergic reaction to this product or any of its ingredients.

Ask Doctor:

Ask a doctor before use if you have - Stomach pain, nausea, vomiting, a sudden change in bowel movements that persists over 2 weeks

ASK DOCTOR/PHARMACIST:

Stop use and ask a doctor if you have:

Rectal bleeding or fail to have a bowel movement after use of a laxative.

These could be signs of a serious condition.

PREGNANCY

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), Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

DIRECTIONS

Take preferably at bedtime or as directed by a doctor.

Dosage

OTHER 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

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 or www.pioneerlifesciences.com

PRINCIPAL DISPLAY PANEL

Label

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:72090-031-101000 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: 8/2020
Document Id: ac8c2ee1-88f3-1490-e053-2a95a90a8d4e
Set id: ac8c3b11-8068-59e6-e053-2a95a90a3256
Version: 1
Effective Time: 20200810
 
Pioneer Life Sciences, LLC