NDC 43689-0056 Tattoo Goo

Chloroxylenol

NDC Product Code 43689-0056

NDC 43689-0056-1

Package Description: 59.15 mL in 1 TUBE

NDC Product Information

Tattoo Goo with NDC 43689-0056 is a a human over the counter drug product labeled by The Magni Group Inc. The generic name of Tattoo Goo is chloroxylenol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: The Magni Group Inc

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug 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.

Tattoo Goo Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • CHLOROXYLENOL .5 mg/100mL

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.

  • SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • WATER (UNII: 059QF0KO0R)
  • POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
  • COCO MONOETHANOLAMIDE (UNII: C80684146D)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • OLIVE OIL POLYGLYCERYL-6 ESTERS (UNII: 4KDO9AFM9I)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: The Magni Group Inc
Labeler Code: 43689
FDA Application Number: part333E What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 08-25-2020 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: N 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.

Tattoo Goo 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: Chloroxylenol 0.5% Purpose: Antibacterial

NDC: 43689-0056-1

Purpose: Antibacterial

NDC: 43689-0056-1

Use: Helps Eliminate Germs On Skin

NDC: 43689-0056-1

Warnings: For External Use Only

NDC: 43689-0056-1

When Using This Product: -Avoid Contact With Eyes -In Case Of Eye Contact, Flush With Water

NDC: 43689-0056-1

Stop Use And Ask A Doctor If Irritation Or Redness Develops.

NDC: 43689-0056-1

Keep Out Of The Reach Of Children. If Swallowed, Get Medical Help Or Contact A Poison Control Center Right Away.

NDC: 43689-0056-1

Directions -Three To Four Times Daily For Tattoos, One To Two Times Daily For Piercings. -Squeeze Into Palm Of Hand. -Work Up Lather In Hands. -Gently Rub Lather Over Tattoo Or Piercing. -Cold Water Rinse, Pat, Then Air Dry.

NDC: 43689-0056-1

Inactive Ingredients: Water (Aqua), Sodium Peg-7 Olive Oil Carboxylate, Propanediol, Olive Oil Peg-7 Esters, Sodium Laureth Sulfate, Polyquaternium 10, Cocoamide Mea, Cocamidopropyl Betaine, Diazolidinyl Urea, Sodium Benzoate, Potassium Sorbate, Citric Acid.

NDC:43689-0056-1

* Please review the disclaimer below.