NDC 53727-102 Premium Gold Mineral Bb

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:
53727-102
Proprietary Name:
Premium Gold Mineral Bb
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
53727
Start Marketing Date: [9]
05-28-2014
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 53727-102?

The NDC code 53727-102 is assigned by the FDA to the product Premium Gold Mineral Bb which is product labeled by Cosmecca Korea Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53727-102-01 50 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 Premium Gold Mineral Bb?

ElishacoyNoblesse NaturalismPremium Gold Mineral BB- Nutrition-rich caviar, royal jelly extract and mineral-rich deep sea water make your skin glossy.- Gold ingredients, Cammelia Japonica Flower extract and Trehalose care for skin trouble, and make your skin moist.- Marine collagen and amino acid complex make your skin elastic by caring for the wrinkles, and approved whitening ingredients make your skin splendid.- This product is a low irritating BB cream that does not contain organic UV absorbing agent that may irritate your skin, but contains ECOCERT-awarded lavender extract and camomile extract.Owing to the UV double blocking effects of UVA and UVB with SPF45 PA+++, the product prevents melanin formation and loss of skin elasticity.

Which are Premium Gold Mineral Bb UNII Codes?

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

Which are Premium Gold Mineral Bb 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".