NDC 69164-3002 Jci Mn Colloidal Iodine Eye Wash Cleansing Water (quasi Drug)

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:
69164-3002
Proprietary Name:
Jci Mn Colloidal Iodine Eye Wash Cleansing Water (quasi Drug)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
69164
Start Marketing Date: [9]
02-01-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 69164-3002?

The NDC code 69164-3002 is assigned by the FDA to the product Jci Mn Colloidal Iodine Eye Wash Cleansing Water (quasi Drug) which is product labeled by Jci Institute Of Medical Science. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69164-3002-1 30 ml in 1 bottle, plastic . 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 Jci Mn Colloidal Iodine Eye Wash Cleansing Water (quasi Drug)?

Apply eyewash several times a day in case of ophthalmic disordersadjust the mumber of times being applying the eye drop, depending on sympthoit is better to increase the number of times for the quick recoveryfor the intranasal disease, it is recommended to apply the drops several times a dayfor the intra-oral disease, keep the drop in the mouth or use as toothpaste

Which are Jci Mn Colloidal Iodine Eye Wash Cleansing Water (quasi Drug) UNII Codes?

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

Which are Jci Mn Colloidal Iodine Eye Wash Cleansing Water (quasi Drug) 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:

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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".