NDC 90069-203 Purpleu Glow Tone It Like Snow

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:
90069-203
Proprietary Name:
Purpleu Glow Tone It Like Snow
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Purple U Co., Ltd
Labeler Code:
90069
Start Marketing Date: [9]
09-02-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 90069-203-01

Package Description: 35 mL in 1 BOTTLE

Product Details

What is NDC 90069-203?

The NDC code 90069-203 is assigned by the FDA to the product Purpleu Glow Tone It Like Snow which is product labeled by Purple U Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 90069-203-01 35 ml in 1 bottle . 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 Purpleu Glow Tone It Like Snow?

Apply liberally 15 minutes before sun exposureReapply at least every 2 hoursUse 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 sun, especially from 10a.m.–2 p.m.Wear long-sleeved shirts, pants, hats, and sunglassesChildren under 6 months: ask a doctor

Which are Purpleu Glow Tone It Like Snow UNII Codes?

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

Which are Purpleu Glow Tone It Like Snow 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".