SENNOSIDES AND DOCUSATE SODIUM- sennosides and docusate sodium tablet 
American Health Packaging

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Sennosides and Docusate Sodium Tablets
Natural Vegetable Laxative with Stool Softener
0462201/0621

Active ingredient (in each tablet)

Docusate Sodium         50 mg
Sennosides            8.6 mg

Purpose

Stool softener
Laxative

Uses

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

Other information

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

8.6 mg/50 mg Sennosides and Docusate Sodium Tablets Carton

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

8.6 mg/50 mg Sennosides and Docusate Sodium Tablet Blister

Sennosides and Docusate
Sodium Tablet
Laxative/Stool Softener

8.6 mg/50 mg

SENNOSIDES AND DOCUSATE SODIUM 
sennosides and docusate sodium tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60687-622(NDC:57896-555)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES8.6 mg
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM50 mg
Inactive Ingredients
Ingredient NameStrength
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
ColororangeScoreno score
ShapeROUNDSize9mm
FlavorImprint Code PSD22
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:60687-622-01100 in 1 BOX, UNIT-DOSE08/03/2021
1NDC:60687-622-111 in 1 BLISTER PACK; Type 0: Not a Combination Product
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33408/03/2021
Labeler - American Health Packaging (929561009)
Establishment
NameAddressID/FEIBusiness Operations
American Health Packaging929561009repack(60687-622)

Revised: 8/2022
Document Id: e77b1ac7-d74f-cd0a-e053-2995a90a31fb
Set id: 4b84d5d7-43cf-47bb-af59-088550c3a0bc
Version: 2
Effective Time: 20220830
 
American Health Packaging