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

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

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)

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 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. Values = ‘Y’ or ‘N’.

* 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*)


First Aid Antiseptic


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


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.


  • 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)



*Microdroplet Suspension Technology

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

* Please review the disclaimer below.