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  4. NDC Product Code: 55038-023 Optical Original Eye Drops

NDC 55038-023 Optical Original Eye Drops

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55038-023?
  4. Optical Original Eye Drops 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:
55038-023
Proprietary Name:
Optical Original Eye Drops
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Televisa Consumer Products Usa
Labeler Code:
55038
Product Label ID:
dbe4a0b2-358a-40ad-847e-656d05cceab6
Start Marketing Date: [9]
10-31-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 55038-023?

The NDC code 55038-023 is assigned by the FDA to the product Optical Original Eye Drops which is product labeled by Televisa Consumer Products Usa. The product's dosage form is . The product is distributed in a single package with assigned NDC code 55038-023-15 1 bottle in 1 carton / 15 ml in 1 bottle. 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 Optical Original Eye Drops?

Directionsput 1 to 2 drops in the affected eye(s) up to 4 times daily children under 6 years of age: ask a doctor

Which are Optical Original Eye Drops UNII Codes?

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

  • TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D)
  • TETRAHYDROZOLINE (UNII: S9U025Y077) (Active Moiety)

Which are Optical Original Eye Drops 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 Optical Original Eye Drops?

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:
  • RxCUI: 1052943 - tetrahydrozoline HCl 0.05 % Ophthalmic Solution
  • RxCUI: 1052943 - tetrahydrozoline hydrochloride 0.5 MG/ML Ophthalmic Solution
  • RxCUI: 1052943 - tetrahydrozoline hydrochloride 0.05 % Eye Drops
  • RxCUI: 1052943 - tetrahydrozoline hydrochloride 0.05 % Ophthalmic Solution

* 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".