NDC 50967-410 Nestabs One

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:
50967-410
Proprietary Name:
Nestabs One
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Womens Choice Pharmaceuticals, Llc
Labeler Code:
50967
Start Marketing Date: [9]
07-20-2017
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327 - OPAQUE)
Shape:
OVAL (C48345)
Size(s):
18 MM
Imprint(s):
ONE
Score:
1

Product Packages

NDC Code 50967-410-30

Package Description: 30 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC

Product Details

What is NDC 50967-410?

The NDC code 50967-410 is assigned by the FDA to the product Nestabs One which is product labeled by Womens Choice Pharmaceuticals, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50967-410-30 30 capsule, gelatin coated in 1 bottle, plastic . 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 Nestabs One?

This medication is a multivitamin, mineral, and fatty acid product used to treat or prevent vitamin deficiency before, during, and after pregnancy. Vitamins, minerals, and fatty acids are important building blocks of the body and help keep you in good health. This combination product also contains iron and folic acid. Women of childbearing age should maintain adequate levels of folic acid either through diet or supplements to prevent infant spinal cord defects in the developing baby.

Which are Nestabs One UNII Codes?

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

Which are Nestabs One 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:

* 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".