SENNA-S LAXATIVE WITH STOOL SOFTENER- sennosides tablet 
Basic Drugs, 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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BASIC DRUGS - SENNA-S - LAXATIVE WITH STOOL SOFTENER (0761-0910)

Active ingredient (in each tablet)

Docusate Sodium 50mg

Sennosides from Senna Concentrate 8.6mg

Purpose

Stool softener

Laxative

Uses

Warnings

Do not use

Ask a doctor before use if you have

Stop use and ask a doctor if you have rectal bleeding or you fail to have a bowel movement after use of a laxative. These could be signs of 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 (1-800-222-1222) right away.

Directions

adults and children 12 years of age and over2-4 tablets daily
children 6 to under 12 years1-2 tablets daily
children 2 to under 6 yearsup to tablet daily
children under 2 years of ageask a doctor

Other information

Inactive ingredients

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

Questions?

937-898-4010

PDP

DF1

DF2

SENNA-S  LAXATIVE WITH STOOL SOFTENER
sennosides tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0761-0910
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM50 mg
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES8.6 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColororangeScoreno score
ShapeROUNDSize9mm
FlavorImprint Code PH32
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0761-0910-02100 in 1 BOTTLE; Type 0: Not a Combination Product12/15/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33412/15/2021
Labeler - Basic Drugs, Inc. (052155082)

Revised: 6/2023
Document Id: fe7fc44e-1cc2-713b-e053-6394a90a64c6
Set id: d32b9956-fc04-8d64-e053-2a95a90a17b3
Version: 4
Effective Time: 20230619
 
Basic Drugs, Inc.