NDC 63730-204 Essential Shockeye And Lip

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:
63730-204
Proprietary Name:
Essential Shockeye And Lip
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Natura Bisse International, S.a.
Labeler Code:
63730
Start Marketing Date: [9]
06-04-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - FD&C YELLOW NO. 5)

Product Packages

NDC Code 63730-204-01

Package Description: 15 mL in 1 TUBE

NDC Code 63730-204-02

Package Description: 1.5 mL in 1 TUBE

Product Details

What is NDC 63730-204?

The NDC code 63730-204 is assigned by the FDA to the product Essential Shockeye And Lip which is product labeled by Natura Bisse International, S.a.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 63730-204-01 15 ml in 1 tube , 63730-204-02 1.5 ml in 1 tube . 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 Essential Shockeye And Lip?

This product is used as Uses: Helps prevent sunburn. Higher SPF gives more sunburn protection.Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun. Moderate sun protection product.

Which are Essential Shockeye And Lip UNII Codes?

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

Which are Essential Shockeye And Lip 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".