1. Home
  2. Labeler Index
  3. Soon Skin Care, Inc.
  4. NDC Product Code: 82079-001 Clear Day Soon Sun

NDC 82079-001 Clear Day Soon Sun

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 82079-001?
  5. Clear Day Soon Sun Uses
  6. Active Ingredients UNII Codes
  7. 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:
82079-001
Proprietary Name:
Clear Day Soon Sun
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Soon Skin Care, Inc.
Labeler Code:
82079
Product Label ID:
96bc5c4c-3bba-477e-b5f3-0342cebd4ca3
Start Marketing Date: [9]
05-06-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)

Code Structure Chart

Product Details

What is NDC 82079-001?

The NDC code 82079-001 is assigned by the FDA to the product Clear Day Soon Sun which is product labeled by Soon Skin Care, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 82079-001-30 1 bottle, plastic in 1 box / 30 ml in 1 bottle, plastic, 82079-001-60 1 bottle, plastic in 1 box / 60 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 Clear Day Soon Sun?

Apply generously and evenly to all areas 15 minutes before sun exposureReapply at least every two hoursUse a water resistant sunscreen if swimming or sweatingConsult a doctor before use on children under six months of age

Which are Clear Day Soon Sun UNII Codes?

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

Which are Clear Day Soon Sun 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".