1. Home
  2. Labeler Index
  3. Zhejiang Tianbo Daily Necessities Co.ltd
  4. NDC Product Code: 79901-002 Baimianqianshu Alcohol Wipes

NDC 79901-002 Baimianqianshu Alcohol Wipes

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79901-002?
  4. Baimianqianshu Alcohol Wipes Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
79901-002
Proprietary Name:
Baimianqianshu Alcohol Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zhejiang Tianbo Daily Necessities Co.ltd
Labeler Code:
79901
Product Label ID:
aca4ad99-6d90-1c74-e053-2995a90a1979
Start Marketing Date: [9]
08-12-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 79901-002?

The NDC code 79901-002 is assigned by the FDA to the product Baimianqianshu Alcohol Wipes which is product labeled by Zhejiang Tianbo Daily Necessities Co.ltd. The product's dosage form is . The product is distributed in 21 packages with assigned NDC codes 79901-002-01 1 container in 1 container / 3.8 ml in 1 container, 79901-002-02 5 container in 1 container / 19 ml in 1 container, 79901-002-03 10 container in 1 container / 38 ml in 1 container, 79901-002-04 15 container in 1 container / 57 ml in 1 container, 79901-002-05 20 container in 1 container / 76 ml in 1 container, 79901-002-06 30 container in 1 container / 114 ml in 1 container, 79901-002-07 36 container in 1 container / 136 ml in 1 container, 79901-002-08 40 container in 1 container / 152 ml in 1 container, 79901-002-09 48 container in 1 container / 182 ml in 1 container, 79901-002-10 50 container in 1 container / 190 ml in 1 container, 79901-002-11 56 container in 1 container / 212 ml in 1 container, 79901-002-12 60 container in 1 container / 228 ml in 1 container, 79901-002-13 64 container in 1 container / 243 ml in 1 container, 79901-002-14 70 container in 1 container / 265 ml in 1 container, 79901-002-15 72 container in 1 container / 273 ml in 1 container, 79901-002-16 80 container in 1 container / 304 ml in 1 container, 79901-002-17 90 container in 1 container / 342 ml in 1 container, 79901-002-18 100 container in 1 container / 380 ml in 1 container, 79901-002-19 60 container in 1 drum / 228 ml in 1 container, 79901-002-20 80 container in 1 drum / 304 ml in 1 container, 79901-002-21 100 container in 1 drum / 380 ml in 1 container. 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 Baimianqianshu Alcohol Wipes?

Open the plastic lid, or unveil the label.Ensure the lidor labelis firmly shut after each use to retain moisture and prevent the product from drying.

Which are Baimianqianshu Alcohol Wipes UNII Codes?

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

Which are Baimianqianshu Alcohol 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:

What is the NDC to RxNorm Crosswalk for Baimianqianshu Alcohol Wipes?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

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".