NDC 69578-466 Curx Antimicrobial Gel
NDC Product Code 69578-466
Proprietary Name: Curx Antimicrobial Gel 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 69578 - Global Health Solutions, Llc
- 69578-466 - Curx Antimicrobial Gel
NDC 69578-466-05
Package Description: 5 g in 1 TUBE
NDC 69578-466-45
Package Description: 45 g in 1 TUBE
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)
- 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 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
- Purpose
- Uses
- Warnings
- Ask A Doctor Before Use If You Have
- When Using This Product
- Stop Use And Ask A Doctor If
- Keep Out Of Reach Of Children
- Directions
- Other Information
- Inactive Ingredients
- Questions?
- *Microdroplet Suspension Technology
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.