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  4. NDC Product Code: 94973-002 Disinfecting Wipes

NDC 94973-002 Disinfecting Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 94973-002?
  4. Disinfecting Wipes 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:
94973-002
Proprietary Name:
Disinfecting Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bifone (pinghu) Medical Equipment Co., Ltd
Labeler Code:
94973
Product Label ID:
b481ced0-bb5a-0831-e053-2a95a90aaf00
Start Marketing Date: [9]
11-20-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 94973-002?

The NDC code 94973-002 is assigned by the FDA to the product Disinfecting Wipes which is product labeled by Bifone (pinghu) Medical Equipment Co., Ltd. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 94973-002-01 60 patch in 1 bag / 4 g in 1 patch, 94973-002-02 100 patch in 1 bag / 4 g in 1 patch, 94973-002-03 150 patch in 1 bag / 4 g in 1 patch. 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 Disinfecting Wipes?

Avoid contact with eyes and mouth.If allergy occurs,discontinue use and consult with your doctor.If a child ingests by accident, get medical advice immediately.Please keep it in a cool and dry place

Which are Disinfecting Wipes UNII Codes?

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

Which are Disinfecting Wipes 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".