SENNA SYRUP- natural vegetable laxative liquid

Senna Syrup by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredients

Sennosides 8.8 mg

Purpose

Laxative

Warning

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

Uses

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

Ask a doctor before use if you

have stomach pain, nausea or vomiting
notice a change in bowel habits that last over 2 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.

OTHER SAFETY INFORMATION

Store at controlled room temperature 20-25°C(68-77°F). Excursions permitted 15-30° (59-86°F).
Tamper Evident: Do not use if foil seal over bottle opening is torn, broken or missing.

Inactive Ingredients

Chocolate flavor, methylparaben, propylene glycol, proylparaben, purified water and sucrose

Dosage

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

HOW SUPPLIED

Senna Syrup 8.8 mg/5 mL

• NDC: 63629-9268-1: 237 mL in a BOTTLE

Repackaged/Relabeled by:
Bryant Ranch Prepack, Inc.
Burbank, CA 91504

PRINCIPAL DISPLAY PANEL

Senna Syrup 8.8 mg/5 mL

INGREDIENTS AND APPEARANCE

SENNA SYRUP 
natural vegetable laxative liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63629-9268(NDC:58657-518)
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
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SUCROSE (UNII: C151H8M554)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63629-9268-1	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/04/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M007	09/28/2021

Labeler - Bryant Ranch Prepack (171714327)

Registrant - Bryant Ranch Prepack (171714327)

Establishment
Name	Address	ID/FEI	Business Operations
Bryant Ranch Prepack		171714327	REPACK(63629-9268) , RELABEL(63629-9268)