NDC 73329-0001 All About Soo Sun Stage Coolstick Spf50 Pa

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:
73329-0001
Proprietary Name:
All About Soo Sun Stage Coolstick Spf50 Pa
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
All About Soo
Labeler Code:
73329
Start Marketing Date: [9]
08-31-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73329-0001-1

Package Description: 20 g in 1 PACKAGE

Product Details

What is NDC 73329-0001?

The NDC code 73329-0001 is assigned by the FDA to the product All About Soo Sun Stage Coolstick Spf50 Pa which is product labeled by All About Soo. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73329-0001-1 20 g in 1 package . 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 All About Soo Sun Stage Coolstick Spf50 Pa?

As the last step of skin care, turn the dial on the bottom of container to raise content about 5 millimeters and apply on areas that need UV protection (face, body). Usage/Volume Take an appropriate amount of this pro -duct and apply it evenly on the skin.

Which are All About Soo Sun Stage Coolstick Spf50 Pa UNII Codes?

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

Which are All About Soo Sun Stage Coolstick Spf50 Pa 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".