NDC 74542-010 Welkin 70% Alcohol Antiseptic

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
74542-010
Proprietary Name:
Welkin 70% Alcohol Antiseptic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ningbo Skl International Co.,ltd.
Labeler Code:
74542
Start Marketing Date: [9]
04-29-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 74542-010-01

Package Description: 55 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-02

Package Description: 100 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-03

Package Description: 300 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-04

Package Description: 500 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-05

Package Description: 980 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-06

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-07

Package Description: 1300 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-08

Package Description: 2000 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-09

Package Description: 5000 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-10

Package Description: 236 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-11

Package Description: 30 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-12

Package Description: 50 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-13

Package Description: 60 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-14

Package Description: 80 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-15

Package Description: 150 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-16

Package Description: 250 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-17

Package Description: 560 mL in 1 BOTTLE, PLASTIC

NDC Code 74542-010-18

Package Description: 3800 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 74542-010?

The NDC code 74542-010 is assigned by the FDA to the product Welkin 70% Alcohol Antiseptic which is product labeled by Ningbo Skl International Co.,ltd.. The product's dosage form is . The product is distributed in 18 packages with assigned NDC codes 74542-010-01 55 ml in 1 bottle, plastic , 74542-010-02 100 ml in 1 bottle, plastic , 74542-010-03 300 ml in 1 bottle, plastic , 74542-010-04 500 ml in 1 bottle, plastic , 74542-010-05 980 ml in 1 bottle, plastic , 74542-010-06 1000 ml in 1 bottle, plastic , 74542-010-07 1300 ml in 1 bottle, plastic , 74542-010-08 2000 ml in 1 bottle, plastic , 74542-010-09 5000 ml in 1 bottle, plastic , 74542-010-10 236 ml in 1 bottle, plastic , 74542-010-11 30 ml in 1 bottle, plastic , 74542-010-12 50 ml in 1 bottle, plastic , 74542-010-13 60 ml in 1 bottle, plastic , 74542-010-14 80 ml in 1 bottle, plastic , 74542-010-15 150 ml in 1 bottle, plastic , 74542-010-16 250 ml in 1 bottle, plastic , 74542-010-17 560 ml in 1 bottle, plastic , 74542-010-18 3800 ml in 1 bottle, plastic . 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 Welkin 70% Alcohol Antiseptic?

Place enough product on hand to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Welkin 70% Alcohol Antiseptic UNII Codes?

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

Which are Welkin 70% Alcohol Antiseptic 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 Welkin 70% Alcohol Antiseptic?

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".