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  4. NDC Product Code: 78543-100 Ceravida Fresh

NDC 78543-100 Ceravida Fresh

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 78543-100?
  4. Ceravida Fresh 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:
78543-100
Proprietary Name:
Ceravida Fresh
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
G.clo Co., Ltd
Labeler Code:
78543
Product Label ID:
a71b8b28-1cca-7056-e053-2a95a90aee5f
Start Marketing Date: [9]
06-02-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 78543-100?

The NDC code 78543-100 is assigned by the FDA to the product Ceravida Fresh which is product labeled by G.clo Co., Ltd. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 78543-100-11 10 kg in 1 bottle , 78543-100-22 20 kg in 1 bottle , 78543-100-33 50 kg in 1 bottle , 78543-100-44 100 kg in 1 bottle , 78543-100-55 1000 kg 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 Ceravida Fresh?

- Mix together in the proper proportion with the water in the tenter's water bath.- Ceravida Fresh dosage is different depending on the tenter capacity.- It must be sufficiently mixed with the water at a rate of about 5-10% dosage to process the fabric.

Which are Ceravida Fresh UNII Codes?

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

Which are Ceravida Fresh 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".