SENNA NATURAL RELIEF tablet

Senna Natural Relief by

Drug Labeling and Warnings

Senna Natural Relief by is a Otc medication manufactured, distributed, or labeled by Pioneer Life Sciences, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

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

INGREDIENTS AND APPEARANCE

SENNA NATURAL RELIEF 
senna natural relief tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72090-031
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX)	SENNOSIDES	8.6 mg

Inactive Ingredients
Ingredient Name	Strength
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
Color	brown	Score	no score
Shape	ROUND	Size	10mm
Flavor		Imprint Code	none
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72090-031-10	1000 in 1 BOTTLE; Type 0: Not a Combination Product	08/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part334	08/03/2020

Labeler - Pioneer Life Sciences, LLC (014092742)