NDC 82384-0034 Everyday Superstars Spf Discovery Kit

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:
82384-0034
Proprietary Name:
Everyday Superstars Spf Discovery Kit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
82384
Start Marketing Date: [9]
12-17-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 82384-0034?

The NDC code 82384-0034 is assigned by the FDA to the product Everyday Superstars Spf Discovery Kit which is product labeled by System Beauty, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82384-0034-1 1 kit in 1 kit * 15 ml in 1 tube (82384-0036-1) * 30 ml in 1 tube (82384-0037-1) * 15 ml in 1 tube (82384-0035-1). 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 Everyday Superstars Spf Discovery Kit?

Apply generously and evenly 15 minutes before sun exposurereapply at least every 2 hoursuse a water resistant sunscreen if swimming or sweatingSun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 a.m. - 2 p.m.Wear long-sleeved shirts, pants, hats, and sunglassessChildren under 6 months: Ask a doctor.

Which are Everyday Superstars Spf Discovery Kit UNII Codes?

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

Which are Everyday Superstars Spf Discovery Kit 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".