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  4. NDC Product Code: 60123-019 Acuvue Theravision With Ketotifen

NDC 60123-019 Acuvue Theravision With Ketotifen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 60123-019?
  5. Acuvue Theravision With Ketotifen Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
60123-019
Proprietary Name:
Acuvue Theravision With Ketotifen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Johnson & Johnson Vision Care, Inc.
Labeler Code:
60123
Product Label ID:
d222d68c-911e-48a9-9bde-a1ca7e992d18
Start Marketing Date: [9]
02-28-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Size(s):
14 MM

Product Packages

NDC Code 60123-019-30

Package Description: 30 BLISTER PACK in 1 CARTON / 1 DRUG-ELUTING CONTACT LENS in 1 BLISTER PACK

Product Details

What is NDC 60123-019?

The NDC code 60123-019 is assigned by the FDA to the product Acuvue Theravision With Ketotifen which is product labeled by Johnson & Johnson Vision Care, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60123-019-30 30 blister pack in 1 carton / 1 drug-eluting contact lens 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 Acuvue Theravision With Ketotifen?

ACUVUE® Theravision™ with Ketotifen is a daily wear, daily disposable etafilcon A drug-eluting contact lens for prevention ocular itch due to allergic conjunctivitis and correction of refractive ametropia (myopia and hyperopia) in aphakic and/or phakic patients who do not have red eye(s), are suitable for contact lens wear and do not have more than 1 D of astigmatism.The lens contains an H1 histamine receptor antagonist for the prevention of ocular itch due to allergic conjunctivitis. The prevention of itch has been demonstrated to last through 12 hours in clinical trials; however, the lens may be worn for longer than 12 hours in a single day.

Which are Acuvue Theravision With Ketotifen UNII Codes?

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

Which are Acuvue Theravision With Ketotifen 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 Acuvue Theravision With Ketotifen?

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: 2604045 - ketotifen 19 MG Drug-Eluting Contact Lens
  • RxCUI: 2604045 - ketotifen 0.019 MG Drug-Eluting Contact Lens
  • RxCUI: 2604045 - ketotifen 19 MG (as ketotifen fumarate 43 MCG) Drug-Eluting Contact Lens
  • RxCUI: 2604049 - ACUVUE Theravision 19 MCG Drug-Eluting Contact Lens
  • RxCUI: 2604049 - ketotifen 0.019 MG Drug-Eluting Contact Lens [Acuvue Theravision]

* 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".