NDC 73793-0013 Coverqueen All In One Sun Roll

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:
73793-0013
Proprietary Name:
Coverqueen All In One Sun Roll
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
73793
Start Marketing Date: [9]
03-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 73793-0013?

The NDC code 73793-0013 is assigned by the FDA to the product Coverqueen All In One Sun Roll which is product labeled by Skinfarm. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73793-0013-1 40 g 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 Coverqueen All In One Sun Roll?

Directions*Apply liberally 15 minutes before sun exposure*Apply all skin will be exposed to the sun*Reapply *after 80 minutes of swimming or sweating *immediately after towel drying*at least every 2 hours*children under the age of 6 months of age: ask a Doctor*Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: *limit time in the sun, especially from 10 AM to 2 PM *wear long-sleeve shirts, pants, hats, and sunglasses

Which are Coverqueen All In One Sun Roll UNII Codes?

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

Which are Coverqueen All In One Sun Roll 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".