NDC 37205-349 Leader Stool Softener Plus Stimulant Laxative
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 37205 - Cardinal Health
- 37205-349 - Leader Stool Softener Plus Stimulant Laxative
Product Characteristics
Product Packages
Product Details
What is NDC 37205-349?
What are the uses for Leader Stool Softener Plus Stimulant Laxative?
Which are Leader Stool Softener Plus Stimulant Laxative UNII Codes?
The UNII codes for the active ingredients in this product are:
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- DOCUSATE (UNII: M7P27195AG) (Active Moiety)
- SENNOSIDES A AND B (UNII: 1B5FPI42EN)
- SENNOSIDES A AND B (UNII: 1B5FPI42EN) (Active Moiety)
Which are Leader Stool Softener Plus Stimulant Laxative Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)
- ALCOHOL (UNII: 3K9958V90M)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MINERAL OIL (UNII: T5L8T28FGP)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Leader Stool Softener Plus Stimulant Laxative?
- RxCUI: 998740 - sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet
- RxCUI: 998740 - docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet
- RxCUI: 998740 - DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".