NDC 60764-125 3ce White Milk Crea M

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:
60764-125
Proprietary Name:
3ce White Milk Crea M
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nanda Co., Ltd
Labeler Code:
60764
Start Marketing Date: [9]
08-20-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 60764-125-02

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 50 mL in 1 BOTTLE, PLASTIC (60764-125-01)

Product Details

What is NDC 60764-125?

The NDC code 60764-125 is assigned by the FDA to the product 3ce White Milk Crea M which is product labeled by Nanda Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60764-125-02 1 bottle, plastic in 1 carton / 50 ml in 1 bottle, plastic (60764-125-01). 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 3ce White Milk Crea M?

Directions: At the last step of your skin care routine, apply a small amount on neck, arms, legs and any other areas of your body that you wish to brighten your skin tone. Make sure to close the lid after use.

Which are 3ce White Milk Crea M UNII Codes?

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

Which are 3ce White Milk Crea M 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 3ce White Milk Crea M?

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:

* Please review the disclaimer below.

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".