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  4. NDC Product Code: 75823-101 Love Nose Easy Powder

NDC 75823-101 Love Nose Easy Powder

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75823-101?
  4. Love Nose Easy Powder Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
75823-101
Proprietary Name:
Love Nose Easy Powder
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Beijing Taiji Jin Kang Medical Technology Co., Ltd.
Labeler Code:
75823
Product Label ID:
a7cac7be-c7a1-3b5a-e053-2995a90a2dc7
Start Marketing Date: [9]
04-22-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

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Product Details

What is NDC 75823-101?

The NDC code 75823-101 is assigned by the FDA to the product Love Nose Easy Powder which is product labeled by Beijing Taiji Jin Kang Medical Technology Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75823-101-01 10 g in 1 bag . 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 Love Nose Easy Powder?

Clean the nasal cavity, put the product in the box of the nose fumigant and cover it well. The nose absorbs the hot fog. Each bag is fumigated 2-3 times, once in the morning, middle and evening everyday. Pay attention to the distance to avoid scalding or use the boiled water in the medicine bag instead of salt water to wash the nose.

Which are Love Nose Easy Powder UNII Codes?

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

Which are Love Nose Easy Powder 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".