NDC 74029-100 Abbexa Hand Sanitizer

NDC Product Code 74029-100

NDC CODE: 74029-100

Proprietary Name: Abbexa Hand Sanitizer 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.

NDC Code Structure

  • 74029 - Abbexa Ltd

NDC 74029-100-01

Package Description: 100 mL in 1 TUBE

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

NDC Product Information

Abbexa Hand Sanitizer with NDC 74029-100 is a product labeled by Abbexa Ltd. 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: 1305100.

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.

  • CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • WATER (UNII: 059QF0KO0R)
  • TROLAMINE (UNII: 9O3K93S3TK)

Product Labeler Information

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

Labeler Name: Abbexa Ltd
Labeler Code: 74029
Start Marketing Date: 04-02-2020 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: 12-31-2021 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".

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Abbexa Hand Sanitizer Product Label Images

Abbexa Hand Sanitizer 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

Ethanol 75%

Purpose

Antiseptic

Indications & Usage

Use To sterilize and disinfect skin.

Warnings

Warnings For external use only.FLAMMABLE liquid and vapour. Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. Causes serious eye irritation. Keep container tightly closed.Avoid contact with eyes. If contact occurs, immediately rinse eyes with water. Stop use and consult a doctor if irritation and redness persists.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, seek medical assistance.

Dosage & Administration

Directions Apply evenly to hands, then repeatedly rub hands until product has dried. No water required. Do not use on damaged, sensitive or irritated skin. In case of contact, rinse thoroughly with tepid water.

Other

Other Information Proven to be effective at decreasing bacteria. Suitable for repeated use on skin.This product contains ethanol, which can irritate mucous membranes and wounds, and should not be used by those who are allergic to alcohol.

Rinse-FreeQuick DryingAntibacterialAbbexa LTD, Cambridge, UK, CB4 0GJT: +44 1223 755950Abbexa LLC, Houston, TX, USA, 77042T: +1 832 327 7413

Storage And Handling

Storage Do not store above 110°F (43 °C).

Inactive Ingredient

Inactive Ingredients Carbomer, Glycerol, Rose Essence, Distilled Water, Triethanolamine.

* Please review the disclaimer below.