NDC 49794-010 Antibacterial

NDC Product Code 49794-010

NDC CODE: 49794-010

Proprietary Name: Antibacterial What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Product Characteristics

Color(s):
BLUE (C48333)

NDC Code Structure

  • 49794 - Continental Manufacturing Chemist, Inc.

NDC 49794-010-99

Package Description: 1100 L in 1 CONTAINER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Antibacterial with NDC 49794-010 is a product labeled by Continental Manufacturing Chemist, Inc.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1020364.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • 2-ETHYLAMINOETHANOL (UNII: 1G0G2TK41H)
  • CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Continental Manufacturing Chemist, Inc.
Labeler Code: 49794
Start Marketing Date: 09-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Antibacterial Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Use(S)

To decrease bacteria on skin

For External Use Only

Flammable!  Keep away from fire or flame.  Do not use in eyes; if this happens rinse thoroughly with water.

Stop Use And Ask A Doctor If

Irritation or redness develops and persists more than 72 hours.

Keep Out Of Reach Of Children

If ingested get medical help or contact a Poison Control Center right away

Directions

Wet hands thoroughly with product and allow to dry without wiping.  Children under six should be supervised when using this product.

Storage

Do not store above 105F (40C)

Inactive Ingredients

Amino Methyl Propanol, Carbomer, Propylene Glycol, Purified Water

* Please review the disclaimer below.