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  4. NDC Product Code: 83437-001 Oceantears

NDC 83437-001 Oceantears

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83437-001?
  4. Oceantears Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
83437-001
Proprietary Name:
Oceantears
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ocean Tears Llc
Labeler Code:
83437
Product Label ID:
fa6b071e-c868-9975-e053-6394a90a547f
Start Marketing Date: [9]
05-05-2023
End Marketing Date: [10]
05-04-2024
Exclude Flag: [12]
I
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Product Details

What is NDC 83437-001?

The NDC code 83437-001 is assigned by the FDA to the product Oceantears which is product labeled by Ocean Tears Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 83437-001-10 1 bottle, dropper in 1 box / 10 ml in 1 bottle, dropper. 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 Oceantears?

UsesFor the temporary relief of burning and irritation due to dryness of the eye.For use as a lubricant to prevent further irritation or to relieve dryness of the eye.For use as a protectant against further irritation or to relieve dryness of the eye.

Which are Oceantears UNII Codes?

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

Which are Oceantears 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 Oceantears?

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

[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.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[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".