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  4. NDC Product Code: 0642-0075 Select-ob Plus Dha Prenatal Supplement Plus Dha

NDC 0642-0075 Select-ob Plus Dha Prenatal Supplement Plus Dha

.beta.-carotene,Vitamin A Acetate,Ascorbic Acid,Cholecalciferol,.alpha.-tocopherol - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0642-0075?
  5. Select-ob Plus Dha Prenatal Supplement Plus Dha Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

NDC Product Code:
0642-0075
Proprietary Name:
Select-ob Plus Dha Prenatal Supplement Plus Dha
Non-Proprietary Name: [1]
.beta.-carotene, Vitamin A Acetate, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, Dl-, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Levomefolate Calcium, Cobalamin, Iron, Magnesium Oxide, Zinc Oxide, And Doconexant
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]
Exeltis Usa, Inc.
Labeler Code:
0642
Product Label ID:
cb5c567a-8733-4004-832e-de8132b8da9e
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]
04-08-2009
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
YELLOW (C48330 - AMBER)
Shape:
OVAL (C48345)
Size(s):
19 MM
15 MM
Imprint(s):
EV0077
Score:
1
Flavor(s):
BERRY (C73365 - MIXED BERRY)

Code Structure Chart

Product Details

What is NDC 0642-0075?

The NDC code 0642-0075 is assigned by the FDA to the product Select-ob Plus Dha Prenatal Supplement Plus Dha which is a human prescription drug product labeled by Exeltis Usa, Inc.. The generic name of Select-ob Plus Dha Prenatal Supplement Plus Dha is .beta.-carotene, vitamin a acetate, ascorbic acid, cholecalciferol, .alpha.-tocopherol acetate, dl-, thiamine mononitrate, riboflavin, niacinamide, pyridoxine hydrochloride, folic acid, levomefolate calcium, cobalamin, iron, magnesium oxide, zinc oxide, and doconexant. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 0642-0075-30 1 kit in 1 carton * 30 tablet, coated in 1 box * 30 capsule in 1 box. 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 Select-ob Plus Dha Prenatal Supplement Plus Dha?

Select-OB®+DHA is indicated to provide vitamin, mineral, and omega-3 fatty acid supplementation prior to conception, throughout pregnancy, and during the postnatal period for the lactating and non-lactating mother, including individuals with known allergies to fish. Select-OB®+DHA does not contain fish, fish oils, fish proteins or fish byproducts.

Which are Select-ob Plus Dha Prenatal Supplement Plus Dha UNII Codes?

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

Which are Select-ob Plus Dha Prenatal Supplement Plus Dha 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 Select-ob Plus Dha Prenatal Supplement Plus Dha?

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:

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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".