SENNA-S- sennosides 8.6mg and docusate sodium 50mg tablet, film coated 
Proficient Rx LP

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

relieves occasional constipation (irregularity)
generally produces a bowel movement in 6-12 hours

Warnings

Do not use

laxative products for longer than 1 week unless directed by a doctor
if you are taking mineral oil, unless directed by a doctor

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

take preferably at bedtime or as directed by a doctor

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

each tablet contains 10 mg of calcium, sodium 5 mg
store at 25°(77°F); excursions permitted between 15o-30oC (59o-86oF)

Inactive ingredients

crosscarmellose 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?

(866) 562-2756 Mon-Fri 8 AM to 4 PM EST

NDC 71205-970-30

Manufactured in the USA

*Compare to the active ingredients in Senokot-S®

SENNA-S

Sennosides 8.6mg &

Docusate Sodium 50mg

Natural Vegetable Laxative

Ingredient Plus Stool Softner

30 TABLETS

Repackaged & Relabele by:

Proficient Rx LP

Thousand Oaks, CA 91320

71205-970-30
SENNA-S 
sennosides 8.6mg and docusate sodium 50mg tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71205-970(NDC:16103-378)
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)  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (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
Colororange (ORANGE COLOR) Scoreno score
ShapeROUND (ROUND TABLET) Size10mm
FlavorImprint Code PH32
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71205-970-3030 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2020
2NDC:71205-970-6060 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2020
3NDC:71205-970-9090 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2020
4NDC:71205-970-00100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2020
5NDC:71205-970-55500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2020
6NDC:71205-970-111000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33411/05/2018
Labeler - Proficient Rx LP (079196022)
Establishment
NameAddressID/FEIBusiness Operations
Proficient Rx LP079196022REPACK(71205-970) , RELABEL(71205-970)

Revised: 6/2020
Document Id: 8678a3ee-0e2c-4c95-ad2e-83aa601f3238
Set id: 8678a3ee-0e2c-4c95-ad2e-83aa601f3238
Version: 1
Effective Time: 20200601
 
Proficient Rx LP