SENNOSIDES AND DOCUSATE SODIUM tablet

Sennosides and Docusate Sodium by

Drug Labeling and Warnings

Sennosides and Docusate Sodium by is a Otc medication manufactured, distributed, or labeled by American Health Packaging. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Docusate Sodium         50 mg
Sennosides            8.6 mg

Purpose

Stool softener
Laxative

Uses

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

Warnings

Do not use for more than one week unless directed by a doctor.

Ask a doctor before use if you

• have abdominal pain, nausea or vomiting
• are taking mineral oil
• have noticed a sudden change in bowel habits that lasts over two 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.

Directions

• do not exceed 8 tablets in 24 hours
• Adults and children 12 years of age and older take 2 tablets once a day preferably at bedtime; increase as needed, or as directed by a doctor; the maximum dose should be 4 tablets in the morning and 4 tablets at bedtime
• Children under 12 years ask a doctor

Other information

• each tablet contains: calcium 20 mg, sodium 3 mg
• store at controlled room temperature
• Keep this and all drugs out of reach of children.
• FOR YOUR PROTECTION: Do not use if blister is torn or broken.

Inactive ingredients

cellulose, croscarmellose sodium, dicalcium phosphate, FD&C yellow #6 lake, hypromellose, magnesium stearate, PEG, silica, talc, titanium dioxide.

PACKAGING INFORMATION

The drug product contained in this package is from NDC # 57896-555, Geri-Care Pharmaceuticals Corp.

Distributed by:
American Health Packaging, Columbus, Ohio 43217

762201
0462201/0621A

Package/Label Display Panel – Carton – 8.6 mg/50 mg

NDC 60687- 622-01

Sennosides* and Docusate Sodium Tablets
Natural Vegetable Laxative with Stool Softener
*Standardized Senna Concentrate

8.6 mg/50 mg

100 Tablets (10 x 10)

Drug Facts
Active ingredients (in each tablet)......................................................................Purpose
Docusate Sodium 50 mg...............................................................................Stool softener
Sennosides 8.6 mg............................................................................................... Laxative

The drug product contained in this package is from
NDC # 57896-555, Geri-Care Pharmaceuticals Corp.

Distributed by:
American Health Packaging, Columbus, Ohio 43217

762201
0462201/0621A

Package/Label Display Panel – Blister – 8.6 mg/50 mg

Sennosides and Docusate
Sodium Tablet
Laxative/Stool Softener

8.6 mg/50 mg

INGREDIENTS AND APPEARANCE

SENNOSIDES AND DOCUSATE SODIUM 
sennosides and docusate sodium tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60687-622(NDC:57896-555)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX)	SENNOSIDES	8.6 mg
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG)	DOCUSATE SODIUM	50 mg

Inactive Ingredients
Ingredient Name	Strength
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	orange	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	PSD22
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60687-622-01	100 in 1 BOX, UNIT-DOSE	08/03/2021
1	NDC: 60687-622-11	1 in 1 BLISTER PACK; 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	08/03/2021

Labeler - American Health Packaging (929561009)

Establishment
Name	Address	ID/FEI	Business Operations
American Health Packaging		929561009	repack(60687-622)