NDC 69578-466 Curx Antimicrobial Gel

NDC Product Code 69578-466

NDC 69578-466-05

Package Description: 5 g in 1 TUBE

NDC 69578-466-45

Package Description: 45 g in 1 TUBE

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

NDC Product Information

Curx Antimicrobial Gel with NDC 69578-466 is a product labeled by Global Health Solutions, Llc. The generic name of Curx Antimicrobial Gel is . The product's dosage form is and is administered via form.

Labeler Name: Global Health Solutions, Llc

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)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • POLIHEXANIDE (UNII: 322U039GMF)

Product Labeler Information

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

Labeler Name: Global Health Solutions, Llc
Labeler Code: 69578
Start Marketing Date: 10-28-2015 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.

Curx Antimicrobial Gel Product Label Images

Curx Antimicrobial Gel 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 Ingredients

Benzalkonium Ch. 0.13% (i/s*)

Purpose

First Aid Antiseptic

Uses

  • First aid to to help treat, protect and prevent skin infection associated withminor cutsscrapesburns

Warnings

For external use only

Ask A Doctor Before Use If You Have

  • Deep or puncture woundsanimal bitesserious burns

When Using This Product

  • Do not use in or near the eyesdo not use if you have a history of allergy to any of the ingredients.

Stop Use And Ask A Doctor If

  • Condition worsens symptoms persist for more than 7 days, or clear up and occur again within a few days.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 2 years and older: clean the affected area; apply a small amount on the area 1-3 times daily;may be covered with a sterile bandage (let dry first)children under 2 years: ask a doctor

Other Information

Avoid excessive heat

Inactive Ingredients

USP Petrolatum, Water, Polihexanide (PHMB)

Questions?

1-706-844-1025

*Microdroplet Suspension Technology

*Proprietary microdroplet suspension technology. Percentage reflective of active ingredient bioavailability in solution.

* Please review the disclaimer below.