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  4. NDC Product Code: 71702-110 Clematis Morning Dew Cc

NDC 71702-110 Clematis Morning Dew Cc

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71702-110?
  4. Clematis Morning Dew Cc 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:
71702-110
Proprietary Name:
Clematis Morning Dew Cc
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Coshub Co., Ltd.
Labeler Code:
71702
Product Label ID:
655d52ed-976c-4f22-94c4-667a188012b2
Start Marketing Date: [9]
08-01-2017
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71702-110-02

Package Description: 1 TUBE in 1 CARTON / 50 mL in 1 TUBE (71702-110-01)

Product Details

What is NDC 71702-110?

The NDC code 71702-110 is assigned by the FDA to the product Clematis Morning Dew Cc which is product labeled by Coshub Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71702-110-02 1 tube in 1 carton / 50 ml in 1 tube (71702-110-01). 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 Clematis Morning Dew Cc?

This product is used as Purpose: Sunscreen

Which are Clematis Morning Dew Cc UNII Codes?

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

Which are Clematis Morning Dew Cc 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".