SENNA TIME- sennosides tablet, coated

SENNA TIME by

Drug Labeling and Warnings

SENNA TIME by is a Otc medication manufactured, distributed, or labeled by Bryant Ranch Prepack. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Each tablet contains:  Sennosides 8.6 mg

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 right away

PURPOSE

PURPOSE:  LAXATIVE

INDICATIONS & USAGE

Relieves occasional constipation (irregularity;generally causes bowel movement in 6-12 hours

DOSAGE & ADMINISTRATION

Directions: Take preferably at bedtime or as directed by a doctor; if you do not have a comfortable bowel movement by the second day, increase dose by one tablet (do not exceed maximum dosage) or decrease dose until you are comfortable.Adults and children 12 years and over - starting dosage: 2 tablets once a day Maximum dosage: 4 tablets twice a dayChildren 6 to under 12 years - starting dosage: 1 tablet once a day Maximum dosage: 2 tablets twice a dayChildren 2 to under 6 years - starting dosage: 1/2 tablet once a day Maximum dosage: 1 tablet twice a dayChildren under 2 years - ask a doctor

WARNINGS

WARNINGS:  Do not use laxative products for longer than 1 week unless directed by a doctor

INACTIVE INGREDIENT

 Inactive Ingredients: croscarmellose sodium, dibasic calcium phosphate dihydrate, hypromellose, magnesium stearate, microcrystalline cellulose, mineral oil

HOW SUPPLIED

Product: 71335-0865

NDC: 71335-0865-1 100 TABLET, COATED in a BOTTLE

NDC: 71335-0865-2 60 TABLET, COATED in a BOTTLE

NDC: 71335-0865-3 120 TABLET, COATED in a BOTTLE

NDC: 71335-0865-4 56 TABLET, COATED in a BOTTLE

NDC: 71335-0865-5 30 TABLET, COATED in a BOTTLE

NDC: 71335-0865-6 90 TABLET, COATED in a BOTTLE

Sennosides 8.6mg Tablet

INGREDIENTS AND APPEARANCE

SENNA TIME 
sennosides tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71335-0865(NDC:49483-080)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SENNOSIDES A AND B (UNII: 1B5FPI42EN) (SENNOSIDES A AND B - UNII:1B5FPI42EN)	SENNOSIDES A AND B	8.6 mg

Inactive Ingredients
Ingredient Name	Strength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
MINERAL OIL (UNII: T5L8T28FGP)

Product Characteristics
Color	brown	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	TCL080
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71335-0865-1	100 in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2017
2	NDC: 71335-0865-2	60 in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2017
3	NDC: 71335-0865-3	120 in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2017
4	NDC: 71335-0865-4	56 in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2017
5	NDC: 71335-0865-5	30 in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2017
6	NDC: 71335-0865-6	90 in 1 BOTTLE; Type 0: Not a Combination Product	06/16/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part334	05/14/2012

Labeler - Bryant Ranch Prepack (171714327)

Establishment
Name	Address	ID/FEI	Business Operations
Bryant Ranch Prepack		171714327	REPACK(71335-0865) , RELABEL(71335-0865)