SENNA SYRUP- sennosides liquid

Senna Syrup by

Drug Labeling and Warnings

Senna Syrup by is a Otc medication manufactured, distributed, or labeled by Atlantic Biologicals Corps, Geri-Care Pharmaceutical Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Each 5ml Contains

Active Ingredient               Purpose

Sennosides 8.8 mg .............Laxative

WARNINGS

Do not give laxative products to your child for a period longer than 1 week unless directed by a doctor

Directions

Do not exceed recomended dose

Age	Starting Dose	Maximun Dose
Adults and Children 2 years and older	2-3 teaspoons once a day preferably at bedtime; increase as needed or as recomended by a doctor	3 teaspoons in the morning and 3 teaspoons at bedtime
under 12 years of age	ask a doctor	ask a doctor

INDICATIONS

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

PURPOSE

Stimulant Laxative

KEEP OUT OF REACH OF CHILDREN

In case of overdose, get medical help or contact a Poison Control center right away.

INACTIVE INGREDIENT

Ccoa Distillate Flavor, Methyparaben, Natural Chocolate Flavor, Propylene Glycol, Propylparaben, Purified Water, Sucrose

LABEL

INGREDIENTS AND APPEARANCE

SENNA SYRUP 
sennosides liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17856-0452
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX)	SENNOSIDES	8.8 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
COCOA (UNII: D9108TZ9KG)
METHYLPARABEN (UNII: A2I8C7HI9T)
CHOCOLATE HIND (UNII: 5O6C53373W)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHOCOLATE, COCONUT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17856-0452-1	72 in 1 BOX	12/01/2017	10/18/2019
1		5 mL in 1 CUP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part334	12/01/2017

Labeler - Atlantic Biologicals Corps (047437707)

Establishment
Name	Address	ID/FEI	Business Operations
Atlantic Biologicals Corps		047437707	REPACK(17856-0452)

Establishment
Name	Address	ID/FEI	Business Operations
Geri-Care Pharmaceutical Corp		611196254	manufacture(17856-0452)