NDC 50090-2375 Stool Softner

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50090-2375
Proprietary Name:
Stool Softner
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
A-s Medication Solutions
Labeler Code:
50090
Start Marketing Date: [9]
03-01-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
RED (C48326 - TWO TONED- WHITE AND CLEAR RED)
Shape:
OVAL (C48345)
Size(s):
12 MM
Imprint(s):
SCU2
Score:
1

Product Packages

NDC Code 50090-2375-1

Package Description: 100 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Code 50090-2375-2

Package Description: 60 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Code 50090-2375-4

Package Description: 30 CAPSULE, LIQUID FILLED in 1 BOTTLE

Product Details

What is NDC 50090-2375?

The NDC code 50090-2375 is assigned by the FDA to the product Stool Softner which is product labeled by A-s Medication Solutions. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 50090-2375-1 100 capsule, liquid filled in 1 bottle , 50090-2375-2 60 capsule, liquid filled in 1 bottle , 50090-2375-4 30 capsule, liquid filled in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Stool Softner?

Take only by mouth. Doses may be taken as a single daily dose or in divided doses.adults and children 12 years and over                        take 1-3 softgels dailychildren 2 to under 12 years of agetake 1 softgel dailychildren under 2 yearsask a doctor

Which are Stool Softner UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Stool Softner 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:

What is the NDC to RxNorm Crosswalk for Stool Softner?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Patient Education

Stool Softeners


Stool softeners are used on a short-term basis to relieve constipation by people who should avoid straining during bowel movements because of heart conditions, hemorrhoids, and other problems. They work by softening stools to make them easier to pass.
[Learn More]


* Please review the disclaimer below.

Product Footnotes

[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".