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  4. NDC Product Code: 68276-004 Bouton Eye Wash

NDC 68276-004 Bouton Eye Wash

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 68276-004?
  4. Bouton Eye Wash Uses
  5. Active Ingredients UNII Codes
  6. 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:
68276-004
Proprietary Name:
Bouton Eye Wash
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aaxis Pacific
Labeler Code:
68276
Product Label ID:
501f0b6f-f2a5-45cc-9954-dc26f41980d7
Start Marketing Date: [9]
01-15-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 68276-004-02

Package Description: 12 BOTTLE in 1 CARTON / 473 mL in 1 BOTTLE (68276-004-01)

NDC Code 68276-004-04

Package Description: 12 BOTTLE in 1 CARTON / 944 mL in 1 BOTTLE (68276-004-03)

Product Details

What is NDC 68276-004?

The NDC code 68276-004 is assigned by the FDA to the product Bouton Eye Wash which is product labeled by Aaxis Pacific. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 68276-004-02 12 bottle in 1 carton / 473 ml in 1 bottle (68276-004-01), 68276-004-04 12 bottle in 1 carton / 944 ml in 1 bottle (68276-004-03). 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 Bouton Eye Wash?

Uses: For flushing/irrigating the eyes to remove loose foreign material, air pollutants, chlorinated water and to refresh irritated or tired eyes.

Which are Bouton Eye Wash UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Bouton Eye Wash?

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.

[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".