NDC 74084-0011 Dr.libeaute Thermal Spring Water

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:
74084-0011
Proprietary Name:
Dr.libeaute Thermal Spring Water
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ongoong Co Ltd
Labeler Code:
74084
Start Marketing Date: [9]
01-30-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 74084-0011-1

Package Description: 500 mL in 1 BOTTLE

NDC Code 74084-0011-2

Package Description: 100 mL in 1 BOTTLE

Product Details

What is NDC 74084-0011?

The NDC code 74084-0011 is assigned by the FDA to the product Dr.libeaute Thermal Spring Water which is product labeled by Ongoong Co Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 74084-0011-1 500 ml in 1 bottle , 74084-0011-2 100 ml 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 Dr.libeaute Thermal Spring Water?

Clean face and pat dry.pour toner onto the soft side onf pad or your palm and dab over the face, neck, and chest(please refer to the directions on the label)

Which are Dr.libeaute Thermal Spring Water UNII Codes?

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

Which are Dr.libeaute Thermal Spring Water 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".