NDC 53208-602 Ohui Powdery Metal Cushion Compact 01 Light Beige

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:
53208-602
Proprietary Name:
Ohui Powdery Metal Cushion Compact 01 Light Beige
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
53208
Start Marketing Date: [9]
01-25-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 53208-602?

The NDC code 53208-602 is assigned by the FDA to the product Ohui Powdery Metal Cushion Compact 01 Light Beige which is product labeled by Lg Household And Health Care Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53208-602-01 2 container in 1 carton / 15 g in 1 container. 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 Ohui Powdery Metal Cushion Compact 01 Light Beige?

Apply liberally 15 minutes before sun exposure.Use a water resistant sunscreen if swimming or sweating.Reapply at least every 2 hours.Sun Protection Measures. Spending time in the sun increases your risk Of skin cancer and early skin aging. To decrease this risk, regularly use aSunscreen with a Broad Spectrum SPF value of 15 or higher and othersun protection measures including:- Limit time in the sun, especially from 10 a.m. to 2 p.m.- Wear longsleeved shirts, pants, hats, and sunglasses.Children under 6 months: Ask a doctor.

Which are Ohui Powdery Metal Cushion Compact 01 Light Beige UNII Codes?

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

Which are Ohui Powdery Metal Cushion Compact 01 Light Beige 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".