SENNA PLUS- sennosides 8.6mg and docusate sodium 50mg tablet, film coated 
SDA Laboratories, Inc.

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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Drug Facts

Active ingredients (in each tablet)

Sennosides from Senna Concentrate 8.6mg

Docusate Sodium 50mg

Purpose

Laxative

Stool softner

Uses

Warnings

Do not use

Ask a doctor before use if you have

  • stomach pain
  • nausea
  • vomiting
  • noticed a sudden change in bowel habits that continues over a period of 2 weeks

Stop use and ask a doctor if

you have rectal bleeding or fail to have a bowel movement after the use of a laxative. These may indicate a serious condition.

If pregnant or breast feeding,

ask a healthcare professional before use. 

Keep out of reach of children.

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

Directions

age

starting dosage

maximum dosage

Adults and children 12 years and over

2 tablets once a day 

4 tablets twice a day

Children 6 to under 12 years

1 tablet once a day

2 tablets  twice a day

Children 2 to under 6 years 

1/2 tablet  once a day

1 tablet twice a day

Children under 2 years

ask a doctor

ask a  doctor

Other information

Inactive ingredients

croscarmellose Sodium, D&C Yellow# 10, dicalcium phosphate, FD&C Yellow #6, magnesium stearate, microcrystalline cellulose, polyvinyl alcohol, polyethylene glycol, sodium benzoate, talc, titanium dioxide

Questions or comments?

(800) 687-0176 Mon-Fri 8 AM to 4 PM EST

NDC 66424-378-02

*Compare to the active ingredients in Senokot-S®

Senna Plus

Natural Vegetable laxative

Ingredient Plus Stool Softener

SENNOSIDES 8.6 mg &

DOCUSATE SODIUM 50mg

SDA LABORATORIES

20 Tablets Free!!

120 Tablets

SDA Senna Plus Tablet 120 ct. Product Label Image

SENNA PLUS 
sennosides 8.6mg and docusate sodium 50mg tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66424-378
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
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColororangeScoreno score
ShapeROUNDSize10mm
FlavorImprint Code PH32
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66424-378-02120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33404/15/2019
Labeler - SDA Laboratories, Inc. (948067889)
Registrant - Pharbest Pharmaceuticals, Inc. (557054835)
Establishment
NameAddressID/FEIBusiness Operations
Pharbest Pharmaceuticals, Inc.557054835manufacture(66424-378) , analysis(66424-378) , pack(66424-378) , label(66424-378)

Revised: 4/2019
Document Id: ac46f272-e4d0-4f13-96b1-78efe697626a
Set id: 08d80e96-c605-40d5-bfb3-e5758daeec80
Version: 1
Effective Time: 20190415
 
SDA Laboratories, Inc.