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  4. NDC Product Code: 69424-280 A Breath Of Fresh Air

NDC 69424-280 A Breath Of Fresh Air

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69424-280?
  4. A Breath Of Fresh Air 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:
69424-280
Proprietary Name:
A Breath Of Fresh Air
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sansung Life & Science Co., Ltd.
Labeler Code:
69424
Product Label ID:
e2540f89-fae8-49bd-bf12-4eb8621a8e4a
Start Marketing Date: [9]
03-01-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69424-280-01

Package Description: 25 mL in 1 CELLO PACK

Product Details

What is NDC 69424-280?

The NDC code 69424-280 is assigned by the FDA to the product A Breath Of Fresh Air which is product labeled by Sansung Life & Science Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69424-280-01 25 ml in 1 cello pack . 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 A Breath Of Fresh Air?

Indication and usage: Step 1. Remove mask from the pouch and gently unfold. Step 2. Apply mask to cleansed skin and smooth to fit contours of face. Step 3. Leave on for 10~15 minutes. Step 4. Discard mask and lightly pat face to help absorb serum into skin.

Which are A Breath Of Fresh Air UNII Codes?

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

Which are A Breath Of Fresh Air 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".