SENNA PLUS- sennosides and docusate sodium tablet, film coated 
Bryant Ranch Prepack

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Active ingredient (in each tablet)

Docusate Sodium 50 mg
Sennosides 8.6 mg

Purpose

Stool softener

Laxative

Uses

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

Warnings

Do not use for more than 1 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 2 weeks

Stop use and ask a doctor if -you have no bowel movement within 12 hours -you have rectal bleeding. these could 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 right away.

Directions

• do not exceed 8 tablets in 24 hours

Age
Starting Dose
Maximum Dose
adults and children 12 years of age and older
2 tablets once a day preferably at bedtime; increase as needed, or as directed by a doctor
4 tablets in the morning and 4 tablets at bedtime
children under 12 years
ask a doctor

Other information

each tablet contains: calcium 7 mg

• store at room temperature

Inactive ingredients

cellulose, croscarmellose sodium, dicalcium phosphate, FD and C yellow no. 5 (tartrazine), FD and C yellow no. 6, hypromellose, magnesium silicate, magnesium stearate, mineral oil, PEG, sodium benzoate, sodium lauryl sulfate, starch, stearic acid, titanium dioxide, triacetin

HOW SUPPLIED

NDC: 71335-0977-1: 30 Tablets in a BOTTLE

NDC: 71335-0977-2: 120 Tablets in a BOTTLE

NDC: 71335-0977-3: 60 Tablets in a BOTTLE

NDC: 71335-0977-4: 90 Tablets in a BOTTLE

NDC: 71335-0977-5: 100 Tablets in a BOTTLE

NDC: 71335-0977-6: 28 Tablets in a BOTTLE

NDC: 71335-0977-7: 56 Tablets in a BOTTLE

NDC: 71335-0977-8: 14 Tablets in a BOTTLE

NDC: 71335-0977-9: 20 Tablets in a BOTTLE

Docusate/ Sennosides 50/8.6 mg Tablet

Label
SENNA PLUS 
sennosides and docusate sodium tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71335-0977(NDC:57896-455)
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
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
TALC (UNII: 7SEV7J4R1U)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIACETIN (UNII: XHX3C3X673)  
Product Characteristics
ColoryellowScoreno score
ShapeROUNDSize10mm
FlavorImprint Code CPC;490
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71335-0977-130 in 1 BOTTLE; Type 0: Not a Combination Product11/20/2019
2NDC:71335-0977-2120 in 1 BOTTLE; Type 0: Not a Combination Product11/09/2018
3NDC:71335-0977-360 in 1 BOTTLE; Type 0: Not a Combination Product12/04/2018
4NDC:71335-0977-490 in 1 BOTTLE; Type 0: Not a Combination Product06/29/2022
5NDC:71335-0977-5100 in 1 BOTTLE; Type 0: Not a Combination Product11/07/2018
6NDC:71335-0977-628 in 1 BOTTLE; Type 0: Not a Combination Product11/28/2018
7NDC:71335-0977-756 in 1 BOTTLE; Type 0: Not a Combination Product06/29/2022
8NDC:71335-0977-814 in 1 BOTTLE; Type 0: Not a Combination Product06/29/2022
9NDC:71335-0977-920 in 1 BOTTLE; Type 0: Not a Combination Product06/29/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00701/01/200004/01/2020
Labeler - Bryant Ranch Prepack (171714327)
Registrant - Bryant Ranch Prepack (171714327)
Establishment
NameAddressID/FEIBusiness Operations
Bryant Ranch Prepack171714327REPACK(71335-0977) , RELABEL(71335-0977)

Revised: 1/2024
 
Bryant Ranch Prepack