NDC 76273-002 Antibacterial Hand Mousse

NDC Product Code 76273-002

NDC 76273-002-03

Package Description: 250 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Antibacterial Hand Mousse with NDC 76273-002 is a product labeled by Mayborn Usa, Inc.. The generic name of Antibacterial Hand Mousse is . The product's dosage form is and is administered via form.

Labeler Name: Mayborn Usa, Inc.

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)
  • COCO GLUCOSIDE (UNII: ICS790225B)
  • COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)

Product Labeler Information

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

Labeler Name: Mayborn Usa, Inc.
Labeler Code: 76273
Start Marketing Date: 07-28-2011 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 Hand Mousse Product Label Images

Antibacterial Hand Mousse 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

Otc - Active Ingredient

Active ingredientBenzalkonium Chloride 0.13%

Otc - Purpose

PurposeAntimicrobial

Indications & Usage

UsesFor hand washing to decrease bacteria on skin.Recommended for repeated use.

Warnings

WarningsFor external use only.

Otc - When Using

When using this product avoid contact with eyes.In case of eye contact, flush eyes with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

DirectionsPump a small amount of foam into the palm of handRub thoroughly over all surfaces of both hands for 15 secondsRinse with potable water.

Inactive Ingredient

Inactive ingredientsWater, coco-glucoside, laurtrimonium chloride, cocamidopropylamine oxide.

* Please review the disclaimer below.