Senna Syrup by Kesin Pharma Corporation SENNA SYRUP syrup

Senna Syrup by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient (per 5 mL)

Sennosides 8.8 mg

Purpose

Laxative

Uses

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

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
• vomiting
• noticed a sudden change in bowel habits that has continued for more than 2 weeks

Stop use and ask a doctor if

• you have rectal bleeding or failure to have a bowel movement after use of a laxative.

These could be a sign of a serious condition.

Keep out of reach of children.

If pregnant or breast-feeding,

ask a health professional before use.

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

Directions

• shake well before use
• do not exceed recommended dose

Age	Starting Dose	Maximun Dose
adults and children; 12 years of age and over	10 mL to 15 mL once a day; preferably at bedtime; increase as needed or; as recommended 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°C to 25°C (68°F to 77°F). [See USP Controlled Room Temperature]
• protect from light and moisture
• a dark brown, cherry flavored syrup supplied in the following:

NDC: 81033-120-05: 5 mL unit dose cup
NDC: 81033-120-50: Carton containing 50 (5 mL unit dose cups)

Inactive ingredients

cherry flavor, citric acid, methylparaben, monoammonium glycyrrhizinate, potassium citrate, propylene glycol, propylparaben, purified water, sorbitol, sucralose

Questions or comments?

Call 1-833-537-4679

SPL UNCLASSIFIED SECTION

Packaged by:
Kesin Pharma
Oldsmar, FL 34677
Rev. 05/2025

PRINCIPAL DISPLAY PANEL

NDC: 81033-120-50

Senna Syrup, USP

8.8 mg Sennosides per 5 mL

Delivers 5 mL

FOR INSTITUTIONAL USE ONLY

INGREDIENTS AND APPEARANCE

SENNA SYRUP 
senna syrup syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81033-120(NDC:84447-120)
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
POTASSIUM CITRATE (UNII: EE90ONI6FF)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
METHYLPARABEN (UNII: A2I8C7HI9T)
SORBITOL (UNII: 506T60A25R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CITRIC ACID (UNII: 2968PHW8QP)
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
WATER (UNII: 059QF0KO0R)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Characteristics
Color	brown (Dark Brown)	Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81033-120-50	50 in 1 CARTON	05/26/2025
1	NDC: 81033-120-05	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	05/26/2025

Labeler - Kesin Pharma Corporation (117447816)

Establishment
Name	Address	ID/FEI	Business Operations
Kesin Pharma Corporation		117447816	label(81033-120) , pack(81033-120) , repack(81033-120)