NDC 75446-111 Medshield Products

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:
75446-111
Proprietary Name:
Medshield Products
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hwl Holdings, Llc
Labeler Code:
75446
Start Marketing Date: [9]
04-27-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 75446-111-02

Package Description: 18 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-04

Package Description: 30 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-06

Package Description: 50 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-08

Package Description: 60 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-10

Package Description: 75 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-12

Package Description: 80 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-14

Package Description: 100 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-16

Package Description: 118 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-18

Package Description: 236 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-20

Package Description: 250 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-22

Package Description: 473 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-24

Package Description: 946 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-26

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-28

Package Description: 1183 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-30

Package Description: 1892 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-32

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-34

Package Description: 10000000 mL in 1 BOTTLE, PLASTIC

NDC Code 75446-111-36

Package Description: 12000000 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 75446-111?

The NDC code 75446-111 is assigned by the FDA to the product Medshield Products which is product labeled by Hwl Holdings, Llc. The product's dosage form is . The product is distributed in 18 packages with assigned NDC codes 75446-111-02 18 ml in 1 bottle, plastic , 75446-111-04 30 ml in 1 bottle, plastic , 75446-111-06 50 ml in 1 bottle, plastic , 75446-111-08 60 ml in 1 bottle, plastic , 75446-111-10 75 ml in 1 bottle, plastic , 75446-111-12 80 ml in 1 bottle, plastic , 75446-111-14 100 ml in 1 bottle, plastic , 75446-111-16 118 ml in 1 bottle, plastic , 75446-111-18 236 ml in 1 bottle, plastic , 75446-111-20 250 ml in 1 bottle, plastic , 75446-111-22 473 ml in 1 bottle, plastic , 75446-111-24 946 ml in 1 bottle, plastic , 75446-111-26 1000 ml in 1 bottle, plastic , 75446-111-28 1183 ml in 1 bottle, plastic , 75446-111-30 1892 ml in 1 bottle, plastic , 75446-111-32 3785 ml in 1 bottle, plastic , 75446-111-34 10000000 ml in 1 bottle, plastic , 75446-111-36 12000000 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 Medshield Products?

Rub thoroughly over all surfaces of both hands.Rub hands together briskly until dry.

Which are Medshield Products UNII Codes?

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

Which are Medshield Products 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 Medshield Products?

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".