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  4. NDC Product Code: 70818-004 Isleaf Satin Lip And Cheek Duo Berry Red

NDC 70818-004 Isleaf Satin Lip And Cheek Duo Berry Red

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70818-004?
  4. Isleaf Satin Lip And Cheek Duo Berry Red 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:
70818-004
Proprietary Name:
Isleaf Satin Lip And Cheek Duo Berry Red
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
C3 Co., Ltd.
Labeler Code:
70818
Product Label ID:
5636f97e-88d3-6c64-e054-00144ff8d46c
Start Marketing Date: [9]
08-08-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70818-004-01

Package Description: 4.5 g in 1 APPLICATOR

Product Details

What is NDC 70818-004?

The NDC code 70818-004 is assigned by the FDA to the product Isleaf Satin Lip And Cheek Duo Berry Red which is product labeled by C3 Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70818-004-01 4.5 g in 1 applicator . 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 Isleaf Satin Lip And Cheek Duo Berry Red?

For a gradient effect, apply only at the center and use the side of the cushion applicator to smudge the color outward to the corners of your mouth.For cheeks, dot on cheeks and lightly smooth dotting by fingertip or applicator

Which are Isleaf Satin Lip And Cheek Duo Berry Red UNII Codes?

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

Which are Isleaf Satin Lip And Cheek Duo Berry Red 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".