SENNA SYRUP- sennosides liquid

Senna Syrup by

Drug Labeling and Warnings

Senna Syrup by is a Otc medication manufactured, distributed, or labeled by Rising Pharma Holdings, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Senna Syrup (8.8 mg/5 mL)

Active ingredient per 5 mL(1 Unit Dose) Sennosides 8.8 mg

PURPOSE

Drug Facts

Purpose

Laxative

INDICATIONS & USAGE

Uses

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

WARNINGS

Warnings

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

Ask a doctor before use if you have

• stomach pain, nausea, or vomiting
• noticed a change in bowel habits that lasts over two weeks

Stop use and ask a doctor if you have rectal bleeding or failure to have a bowel movement after use of laxative. These may indicate a serious condition.

PREGNANCY

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222)

DOSAGE & ADMINISTRATION

Directions

• shake well before use
• do not exceed recommended dose

Age	Starting Dose	Maximum Dose
Adults and children over 12 years of age	10 to 15 mL once a day at bedtime, increase as needed or as directed by a doctor	15 mL in the morning and 15 mL at bedtime
Children under 12 years of age	Ask a doctor	Ask a doctor

Other information

store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature]
do not use if lid is torn or broken

INACTIVE INGREDIENT

Inactive ingredients flavor, methylparaben, propylene glycol, propylparaben, purified water, and sucrose.

QUESTIONS

Questions or comments? Call 1-844-474-7464

PRINCIPAL DISPLAY PANEL

Distributed by:

Rising Pharma Holdings, Inc.

East Brunswick, NJ 08816

FG-38/Iss.: 04/2023

Lid Label

Case Label

INGREDIENTS AND APPEARANCE

SENNA SYRUP 
sennosides liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57237-310
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
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHOCOLATE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57237-310-54	40 in 1 BOX	05/23/2023
1	NDC: 57237-310-05	5 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M007.60	05/23/2023

Labeler - Rising Pharma Holdings, Inc. (116880195)