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  4. NDC Product Code: 64058-354 Omega 3

NDC 64058-354 Omega 3

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64058-354?
  4. Omega 3 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
64058-354
Proprietary Name:
Omega 3
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Concept Laboratories, Inc.
Labeler Code:
64058
Product Label ID:
4d5c8d59-a968-4d96-a4a0-04b34ed08596
Start Marketing Date: [9]
07-08-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 64058-354-18

Package Description: 238 g in 1 BOTTLE, PLASTIC

Product Details

What is NDC 64058-354?

The NDC code 64058-354 is assigned by the FDA to the product Omega 3 which is product labeled by Concept Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64058-354-18 238 g 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 Omega 3?

Rotate pump's spout counter-clockwise slightly to unlock; clockwise to lockChildren under 12 years of age consult a physicianApply a thin layer to affected area not more than 3 to 4 times dailyGently massage into the skin until fully absorbedWash hands with soap and water after each application to avoid spreading to the eyes or other sensitive mucous membranes

Which are Omega 3 UNII Codes?

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

Which are Omega 3 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

[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".