Stool Softener with Laxative

Product NDC
71335-2522
11-digit product format
713352522
Labeler code
71335
Product ID
71335-2522_50ff216f-56d0-4d51-ac30-f08ba4e22cf4
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate Sodium and Sennosides
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-12-01
Substance
DOCUSATE SODIUM; SENNOSIDES
Active strength
50; 8.6 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
F05Q2T2JA0DOCUSATE SODIUM577-11-7DOCUSATE SODIUM
3FYP5M0IJXSENNOSIDESSENNOSIDES

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71335-2522-17133525220130 TABLET, FILM COATED in 1 BOTTLE (71335-2522-1) 2024-11-04NoNoHistorical
71335-2522-271335252202120 TABLET, FILM COATED in 1 BOTTLE (71335-2522-2) 2024-11-04NoNoHistorical
71335-2522-37133525220360 TABLET, FILM COATED in 1 BOTTLE (71335-2522-3) 2024-11-04NoNoHistorical
71335-2522-47133525220490 TABLET, FILM COATED in 1 BOTTLE (71335-2522-4) 2024-11-04NoNoHistorical
71335-2522-571335252205100 TABLET, FILM COATED in 1 BOTTLE (71335-2522-5) 2024-11-04NoNoHistorical
71335-2522-67133525220628 TABLET, FILM COATED in 1 BOTTLE (71335-2522-6) 2024-11-04NoNoHistorical
71335-2522-77133525220756 TABLET, FILM COATED in 1 BOTTLE (71335-2522-7) 2024-11-04NoNoHistorical
71335-2522-87133525220814 TABLET, FILM COATED in 1 BOTTLE (71335-2522-8) 2024-11-04NoNoHistorical
71335-2522-97133525220920 TABLET, FILM COATED in 1 BOTTLE (71335-2522-9) 2024-11-04NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Gericare 303B (304)Bryant Ranch Prepack2024-11-04HUMAN OTC DRUG LABEL1