NDC 51523-317 Myeonghan Miindo Hwansaenggo Gold Essence Bb Spf 35 30100317

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:
51523-317
Proprietary Name:
Myeonghan Miindo Hwansaenggo Gold Essence Bb Spf 35 30100317
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Thefaceshop Co. Ltd.
Labeler Code:
51523
Start Marketing Date: [9]
11-20-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51523-317-01

Package Description: 1 TUBE in 1 CARTON / 45 mL in 1 TUBE

Product Details

What is NDC 51523-317?

The NDC code 51523-317 is assigned by the FDA to the product Myeonghan Miindo Hwansaenggo Gold Essence Bb Spf 35 30100317 which is product labeled by Thefaceshop Co. Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51523-317-01 1 tube in 1 carton / 45 ml in 1 tube. 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 Myeonghan Miindo Hwansaenggo Gold Essence Bb Spf 35 30100317?

Reapply at least every 2 hours. Use a water-resistant sunscreen if swimming or sweating. May stain or damage some fabrics or surfaces. Dispense an adequate amount and apply to the face after your skincare routine. 1) After basic makeup, lightly apply an adequate amount of the product all over your face in order of cheek forehead nose chin. 2) Thinly spread out on the T zone and chin to prevent lumps and cup your face with your palms to increase absorption and adhesion.

Which are Myeonghan Miindo Hwansaenggo Gold Essence Bb Spf 35 30100317 UNII Codes?

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

Which are Myeonghan Miindo Hwansaenggo Gold Essence Bb Spf 35 30100317 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".