SENNA SYRUP- sennosides syrup

Senna Syrup by

Drug Labeling and Warnings

Senna Syrup 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 (per 5 mL teaspoon)

Sennosides 8.8 mg

Purpose

Laxative

Uses

• Relieves occasional constipation (irregularity)
• Generally causes bowel movement in 6 to 12 hours

Warnings

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

Ask a doctor before use if you

• have stomach pain, nausea or vomiting
• notice a change in bowel habits that last over two weeks
• are pregnant or breastfeeding

Stop use and ask a doctor if 

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

Keep out of reach of children.

In case of accidental overdose, get medical help or contact a Poison Control Center immediately.

Directions

Shake well before using. Do not exceed maximum dose. Take at bedtime or as directed by a doctor.

Age	Usual Dose	Maximum Dose
Adults & children 12 years and older	2-3 teaspoons once a day	3 teaspoons twice a day
6 to 12 years	1 to 1-1/2 teaspoons once a day	1 1/2 teaspoons twice a day
2 to 6 years	1/2 to 3/4 teaspoon once a day	3/4 teaspoon once a day
Under 2 years	Consult a doctor

Other Information

• store at 20-25°C (68-77°F)

Inactive Ingredients

Propylene Glycol USP, Methyl Paraben NF, Propyl Paraben NF, Sucrose NF, Chocolate Flavor Artificial & Natural, Brownie Flavor Artificial & Natural.

SPL UNCLASSIFIED SECTION

Questions or comments?

Call + 1 (732) 994-2808 or email support@gencare.health

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SENNA SYRUP 
sennosides syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72090-022
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
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SUCROSE (UNII: C151H8M554)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72090-022-01	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/18/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/18/2024

Labeler - Pioneer Life Sciences, LLC (014092742)

Registrant - Pioneer Life Sciences, LLC (014092742)