NDC 71421-501 Olivia Quido Skincare Blemish Eraser

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:
71421-501
Proprietary Name:
Olivia Quido Skincare Blemish Eraser
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
O Skin Care Llc
Labeler Code:
71421
Start Marketing Date: [9]
07-27-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71421-501-30

Package Description: 1 BOTTLE, PUMP in 1 CARTON / 30 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 71421-501?

The NDC code 71421-501 is assigned by the FDA to the product Olivia Quido Skincare Blemish Eraser which is product labeled by O Skin Care Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71421-501-30 1 bottle, pump in 1 carton / 30 ml in 1 bottle, pump. 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 Olivia Quido Skincare Blemish Eraser?

Adults: apply a small amount as a thin layer on the affected area twice daily, or use as directed by a physician. If no improvement is seen after 3 months of treatment, use of this product should be discontinued.Lightening effect of this product may not be noticeable when used on dark skin.Children under 12 years old: do not use unless directed by a physician.Sun exposure should be limited by using a sunscreen agent or protective clothing to cover bleached skin when using and after using this product in order to prevent darkening from reoccurring.

Which are Olivia Quido Skincare Blemish Eraser UNII Codes?

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

Which are Olivia Quido Skincare Blemish Eraser 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:

What is the NDC to RxNorm Crosswalk for Olivia Quido Skincare Blemish Eraser?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".