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  4. NDC Product Code: 71733-101 Qyo Qyo Tangerine Bright Moist All In One Cream

NDC 71733-101 Qyo Qyo Tangerine Bright Moist All In One Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71733-101?
  4. Qyo Qyo Tangerine Bright Moist All In One Cream Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71733-101
Proprietary Name:
Qyo Qyo Tangerine Bright Moist All In One Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lala Co., Ltd.
Labeler Code:
71733
Product Label ID:
94e8c3a3-9194-4464-e053-2a95a90a4ecf
Start Marketing Date: [9]
01-01-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71733-101-01

Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 150 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 71733-101?

The NDC code 71733-101 is assigned by the FDA to the product Qyo Qyo Tangerine Bright Moist All In One Cream which is product labeled by Lala Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71733-101-01 1 bottle, plastic in 1 box / 150 ml in 1 bottle, plastic. 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 Qyo Qyo Tangerine Bright Moist All In One Cream?

• Apply as needed. • After cleansing your face, apply a proper amount on skin and spread lightly for absorption.

Which are Qyo Qyo Tangerine Bright Moist All In One Cream UNII Codes?

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

Which are Qyo Qyo Tangerine Bright Moist All In One Cream 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".