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  4. NDC Product Code: 81630-002 Wash-free Surgical Hand Disinfectant Gel Ii

NDC 81630-002 Wash-free Surgical Hand Disinfectant Gel Ii

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81630-002?
  4. Active Ingredients UNII Codes
  5. Inactive Ingredients UNII Codes
  6. 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:
81630-002
Proprietary Name:
Wash-free Surgical Hand Disinfectant Gel Ii
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shan Dong Lircon Medical Technology Co., Ltd
Labeler Code:
81630
Product Label ID:
8f17e4a0-831a-4fa2-874a-ad946fa3f0cf
Start Marketing Date: [9]
03-31-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81630-002-03

Package Description: 10 BOX in 1 BOX / 10 BOTTLE, PLASTIC in 1 BOX (81630-002-02) / 60 mL in 1 BOTTLE, PLASTIC (81630-002-01)

NDC Code 81630-002-05

Package Description: 40 BOTTLE, PLASTIC in 1 BOX / 248 mL in 1 BOTTLE, PLASTIC (81630-002-04)

NDC Code 81630-002-07

Package Description: 25 BOTTLE, PLASTIC in 1 BOX / 500 mL in 1 BOTTLE, PLASTIC (81630-002-06)

NDC Code 81630-002-09

Package Description: 16 BOTTLE, PLASTIC in 1 BOX / 1000 mL in 1 BOTTLE, PLASTIC (81630-002-08)

NDC Code 81630-002-11

Package Description: 15 BOTTLE, PLASTIC in 1 BOX / 1000 mL in 1 BOTTLE, PLASTIC (81630-002-10)

NDC Code 81630-002-13

Package Description: 5 PACKAGE in 1 BOX / 5000 mL in 1 PACKAGE (81630-002-12)

Product Details

What is NDC 81630-002?

The NDC code 81630-002 is assigned by the FDA to the product Wash-free Surgical Hand Disinfectant Gel Ii which is product labeled by Shan Dong Lircon Medical Technology Co., Ltd. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 81630-002-03 10 box in 1 box / 10 bottle, plastic in 1 box (81630-002-02) / 60 ml in 1 bottle, plastic (81630-002-01), 81630-002-05 40 bottle, plastic in 1 box / 248 ml in 1 bottle, plastic (81630-002-04), 81630-002-07 25 bottle, plastic in 1 box / 500 ml in 1 bottle, plastic (81630-002-06), 81630-002-09 16 bottle, plastic in 1 box / 1000 ml in 1 bottle, plastic (81630-002-08), 81630-002-11 15 bottle, plastic in 1 box / 1000 ml in 1 bottle, plastic (81630-002-10), 81630-002-13 5 package in 1 box / 5000 ml in 1 package (81630-002-12). 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.

Which are Wash-free Surgical Hand Disinfectant Gel Ii UNII Codes?

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

Which are Wash-free Surgical Hand Disinfectant Gel Ii 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 Wash-free Surgical Hand Disinfectant Gel Ii?

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:

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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".