NDC 11673-636 Up And Up Lubricant Refreshing

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
11673-636
Proprietary Name:
Up And Up Lubricant Refreshing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Target Corporation
Labeler Code:
11673
Start Marketing Date: [9]
04-19-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11673-636-70

Package Description: 70 VIAL in 1 CARTON / .4 mL in 1 VIAL

Product Details

What is NDC 11673-636?

The NDC code 11673-636 is assigned by the FDA to the product Up And Up Lubricant Refreshing which is product labeled by Target Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11673-636-70 70 vial in 1 carton / .4 ml in 1 vial. 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 Up And Up Lubricant Refreshing?

Directionsto open, twist and pull tab to removeinstill 1 or 2 drops in the affected eye(s) as neededchildren under 6 years of age: ask a doctor

Which are Up And Up Lubricant Refreshing UNII Codes?

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

  • CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
  • CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X) (Active Moiety)

Which are Up And Up Lubricant Refreshing 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 Up And Up Lubricant Refreshing?

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: 1188426 - carboxymethylcellulose sodium 0.5 % Ophthalmic Solution
  • RxCUI: 1188426 - carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution
  • RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 GM per 100 ML 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".