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  4. NDC Product Code: 81392-001 Phoemay

NDC 81392-001 Phoemay

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81392-001?
  4. Phoemay 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:
81392-001
Proprietary Name:
Phoemay
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Yibin Hmei Kangjian Biotechnology Co., Ltd.
Labeler Code:
81392
Product Label ID:
be179483-13f5-736c-e053-2a95a90a4f27
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 81392-001?

The NDC code 81392-001 is assigned by the FDA to the product Phoemay which is product labeled by Yibin Hmei Kangjian Biotechnology Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81392-001-01 80 cloth in 1 package . 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 Phoemay?

Open the lid and tear the tape, takeout the production to wipe the skin to be cleaned. Please close the lid after use, to avoid moisture evaporation. Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Phoemay UNII Codes?

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

Which are Phoemay 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".