Home NDC 79903-009-12 Stool Softener Laxative
Product NDC 79903-009
Requested package NDC 79903-009-12
11-digit product format 799030009
Labeler code 79903
Product ID 79903-009_ced03150-1efa-4cab-92ca-214d710f1fa2
Type HUMAN OTC DRUG
Nonproprietary name Docusate sodium, Sennosides
Dosage form TABLET
Route ORAL
Labeler WALMART INC. (see also Equate)
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-12-31
Substance DOCUSATE SODIUM; SENNOSIDES
Active strength 50; 8.6 mg/1; mg/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Stool Softener Laxative
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DOCUSATE SODIUM 50 mg/1 SENNOSIDES 8.6 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F05Q2T2JA0 Internal UNII lookup 3FYP5M0IJX Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 998740 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 79903-009-12 Stool Softener Laxative 120 in 1 BOTTLE, PLASTIC TABLET 120 4 79903-009-24 Stool Softener Laxative 240 in 1 BOTTLE, PLASTIC TABLET 240 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79903-009 STOOL SOFTENER LAXATIVE (DOCUSATE SODIUM, SENNOSIDES) TABLET [WALMART INC. (SEE ALSO EQUATE)] 4 Current NDC, Legacy NDC, 2 package rows 20240808_43fd4231-0962-4828-a3fa-a1faec81e43d.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 79903-009-12 79903000912 120 TABLET in 1 BOTTLE, PLASTIC (79903-009-12) 120 tablet 2020-12-31 0000-00-00 No No Current