NDC 72709-821 Lutesol Homeopathic Medicine Sterile Eye Drops

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:
72709-821
Proprietary Name:
Lutesol Homeopathic Medicine Sterile Eye Drops
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Yokina Inc.
Labeler Code:
72709
Start Marketing Date: [9]
11-28-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72709-821-78

Package Description: 1 BOTTLE, DROPPER in 1 BOX / 15 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 72709-821?

The NDC code 72709-821 is assigned by the FDA to the product Lutesol Homeopathic Medicine Sterile Eye Drops which is product labeled by Yokina Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72709-821-78 1 bottle, dropper in 1 box / 15 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 Lutesol Homeopathic Medicine Sterile Eye Drops?

This product is used as Corneal health. According to homeopathic indications these ingredients provide temporary relief from symptoms such as Dryness, redness and promote corneal health, after a serious causes have been ruled out by physician.*These statements are based on traditional homeopathic practice. They have not been reviewed by Food and Drug Administration

Which are Lutesol Homeopathic Medicine Sterile Eye Drops UNII Codes?

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

  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)

Which are Lutesol Homeopathic Medicine Sterile 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:

* 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".