NDC 53727-103 Time Machine 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:
53727-103
Proprietary Name:
Time Machine 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 53727-103?

The NDC code 53727-103 is assigned by the FDA to the product Time Machine 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 53727-103-01 30 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 Time Machine Bb?

ElishaCoyNoblesse NaturalismTime Capsule BBLift that brings your skin back to life- Provides sun protection, whitening, and anti-wrinkle functions all in one balanced cream- Attacks calluses deep inside the skin by revitalizing skin cells- Using mink oil as a key ingredeint, it gives your skin all the moisture and smoothness of the finest mink pelts- Skin wrapping system uses a special adhesive polymer to form a thin film makeup that will last all day long- Enriched ingredients provide skin cells with the energy to produce healthy and bright skin[Effects] Skin whitening, Wrinkle improve ments, UVA/B protection [SPF30 PA++]

Which are Time Machine Bb UNII Codes?

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

Which are Time Machine 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".