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  4. NDC Product Code: 49283-700 Ethyl Alcohol

NDC 49283-700 Ethyl Alcohol

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49283-700?
  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:
49283-700
Proprietary Name:
Ethyl Alcohol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chemco Corporation
Labeler Code:
49283
Product Label ID:
aed085e8-d8aa-671a-e053-2995a90ac9a4
Start Marketing Date: [9]
06-02-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49283-700-01

Package Description: 3785 mL in 1 BOTTLE

NDC Code 49283-700-02

Package Description: 59 mL in 1 BOTTLE, PUMP

NDC Code 49283-700-08

Package Description: 236 mL in 1 BOTTLE, PUMP

NDC Code 49283-700-18

Package Description: 532 mL in 1 BOTTLE, PUMP

NDC Code 49283-700-32

Package Description: 946 mL in 1 BOTTLE

NDC Code 49283-700-64

Package Description: 1892 mL in 1 BOTTLE

Product Details

What is NDC 49283-700?

The NDC code 49283-700 is assigned by the FDA to the product Ethyl Alcohol which is product labeled by Chemco Corporation. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 49283-700-01 3785 ml in 1 bottle , 49283-700-02 59 ml in 1 bottle, pump , 49283-700-08 236 ml in 1 bottle, pump , 49283-700-18 532 ml in 1 bottle, pump , 49283-700-32 946 ml in 1 bottle , 49283-700-64 1892 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.

Which are Ethyl Alcohol UNII Codes?

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

Which are Ethyl Alcohol 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 Ethyl Alcohol?

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".