SENNA- sennosides capsule, liquid filled

SENNA by

Drug Labeling and Warnings

SENNA by is a Otc medication manufactured, distributed, or labeled by RITE AID CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient (in each Softgel)

Sennosides 8.6 mg

Purpose

Laxative

Uses

relieves occasional constipation (irregularity) generally produces bowel movement in 6–12 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 lasts over 2 weeks

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

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

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

Directions

take preferably at bedtime or as directed by a doctor

Age	Starting Dosage	Maximum Dosage
adults & children 12 years of age & over	2 softgels once a day	4 softgels twice a day
children 6 to under 12 years of age	1 softgels once a day	2 softgels twice a day
children under 6 years of age	ask a doctor	ask a doctor

Other information

each softgel contains: calcium 1 mg and sodium less than 1 mg
store at 25°C (77°F); excursions permitted between 15°–30°C (59°–86°F)

Inactive ingredients

aerosil, beeswax, FD&C Blue No. 1, FD&C Red No.40, FD&C Yellow
No. 6, gelatin, glycerin, light liquid paraffin, povidone (PVP K-30), purified water, sodium carboxymethyl cellulose, sorbitol solution, soya lecithin, titanium dioxide

Questions or comments?

1-888-333-9792

SPL UNCLASSIFIED SECTION

Distributed by:
RITE AID
30 Hunter Lane, Camp Hill, PA 17011

www.riteaid.com

Made in India

Label

Carton

INGREDIENTS AND APPEARANCE

SENNA 
sennosides capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-1571
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX)	SENNOSIDES	8.6 mg

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
GELATIN (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
PARAFFIN (UNII: I9O0E3H2ZE)
POVIDONE K30 (UNII: U725QWY32X)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
SORBITOL SOLUTION (UNII: 8KW3E207O2)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	brown	Score	no score
Shape	OVAL	Size	10mm
Flavor		Imprint Code	458
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-1571-6	1 in 1 CARTON	12/28/2021
1		60 in 1 BOTTLE; 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	12/27/2021

Labeler - RITE AID CORPORATION (014578892)