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  4. NDC Product Code: 75734-1090 Sanilso G75

NDC 75734-1090 Sanilso G75

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75734-1090?
  4. Sanilso G75 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:
75734-1090
Proprietary Name:
Sanilso G75
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Four Maples Vineyard & Winery Inc.
Labeler Code:
75734
Product Label ID:
a5a80115-6112-6c84-e053-2a95a90ab231
Start Marketing Date: [9]
05-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 75734-1090-1

Package Description: 1000 mL in 1 BOTTLE

NDC Code 75734-1090-2

Package Description: 4000 mL in 1 JUG

NDC Code 75734-1090-3

Package Description: 189000 mL in 1 PAIL

NDC Code 75734-1090-4

Package Description: 207800 mL in 1 DRUM

NDC Code 75734-1090-5

Package Description: 500 mL in 1 BOTTLE

NDC Code 75734-1090-6

Package Description: 250 mL in 1 BOTTLE

Product Details

What is NDC 75734-1090?

The NDC code 75734-1090 is assigned by the FDA to the product Sanilso G75 which is product labeled by Four Maples Vineyard & Winery Inc.. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 75734-1090-1 1000 ml in 1 bottle , 75734-1090-2 4000 ml in 1 jug , 75734-1090-3 189000 ml in 1 pail , 75734-1090-4 207800 ml in 1 drum , 75734-1090-5 500 ml in 1 bottle , 75734-1090-6 250 ml in 1 bottle . 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 Sanilso G75?

Place enough product on hands 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 Sanilso G75 UNII Codes?

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

Which are Sanilso G75 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:

  • AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • HYDROGEN PEROXIDE (UNII: BBX060AN9V)
  • WATER (UNII: 059QF0KO0R)

* 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".