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  4. NDC Product Code: 50967-317 Nestabs Dha Prenatal Multi-vitamin/mineral Supplement With Dha/epa

NDC 50967-317 Nestabs Dha Prenatal Multi-vitamin/mineral Supplement With Dha/epa

Sodium Ascorbate,Cholecalciferol,Di-alpha-tocopheryl Acetate,Thiamine - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50967-317?
  5. Nestabs Dha Prenatal Multi-vitamin/mineral Supplement With Dha/epa Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
50967-317
Proprietary Name:
Nestabs Dha Prenatal Multi-vitamin/mineral Supplement With Dha/epa
Non-Proprietary Name: [1]
Sodium Ascorbate, Cholecalciferol, Di-alpha-tocopheryl Acetate, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine Hcl, Folic Acid, Cyanocobalamin, Calcium Formate, Calcium Carbonate, Ferrous (ii) Bis-glycinate Chelate, Potassium Iodide, Zinc Oxide, Choline Bitartrate, With Doconexent And Icosapent
NDC Directory Status:
Human Prescription Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Womens Choice Pharmaceuticals Llc
Labeler Code:
50967
Product Label ID:
2dd25bf2-f1a7-4bc4-bdf2-12d9065ea0cf
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date: [9]
02-01-2011
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
YELLOW (C48330)
Shape:
OVAL (C48345)
Size(s):
18 MM
6 MM
Imprint(s):
WC;001
;
Score:
1

Code Structure Chart

Product Details

What is NDC 50967-317?

The NDC code 50967-317 is assigned by the FDA to the product Nestabs Dha Prenatal Multi-vitamin/mineral Supplement With Dha/epa which is a human prescription drug product labeled by Womens Choice Pharmaceuticals Llc. The generic name of Nestabs Dha Prenatal Multi-vitamin/mineral Supplement With Dha/epa is sodium ascorbate, cholecalciferol, di-alpha-tocopheryl acetate, thiamine mononitrate, riboflavin, niacinamide, pyridoxine hcl, folic acid, cyanocobalamin, calcium formate, calcium carbonate, ferrous (ii) bis-glycinate chelate, potassium iodide, zinc oxide, choline bitartrate, with doconexent and icosapent. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 50967-317-30 4 blister pack in 1 carton / 1 kit in 1 blister pack. 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 Dha Prenatal Multi-vitamin/mineral Supplement With Dha/epa?

This medication contains vitamins, minerals, and fatty acids. It is used to treat or prevent a lack of these nutrients during pregnancy or due to poor diet or certain illnesses. Vitamins, minerals, and fatty acids are important building blocks of the body and help keep you in good health. This combination product may contain folic acid. Women who are or may become pregnant should maintain adequate levels of folic acid through either diet or supplements to prevent spinal cord birth defects. Some supplement products have been found to contain possibly harmful impurities/additives. Check with your pharmacist for more details about the brand you use. The FDA has not reviewed this product for safety or effectiveness. Consult your doctor or pharmacist for more details.

Which are Nestabs Dha Prenatal Multi-vitamin/mineral Supplement With Dha/epa UNII Codes?

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

Which are Nestabs Dha Prenatal Multi-vitamin/mineral Supplement With Dha/epa 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:

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Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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".