Skullduggery Pain Relief And Skin Protection For Tattoos
NDC 67234-047

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 67234-047?
  4. Skullduggery Pain Relief And Skin Protection For Tattoos Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

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

Skullduggery Pain Relief And Skin Protection For Tattoos is a OTC MONOGRAPH FINAL-approved product labeled by Natureplex, Llc. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 67234-047 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
67234-047
Proprietary Name:
Skullduggery Pain Relief And Skin Protection For Tattoos
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Natureplex, Llc
Labeler Code:
67234
Product Label ID:
d61ed5a0-c814-4822-9ea1-7244dedaa197
FDA Application Number: [6]
part347
Marketing Category: [8]
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.

Marketing Timeline

Start Marketing Date: [9]
06-04-2003
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 67234-047?

The NDC code 67234-047 is assigned by the FDA to the product Skullduggery Pain Relief And Skin Protection For Tattoos. This pharmaceutical product is labeled by Natureplex, Llc and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 67234-047-01. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

For adult use onlybefore procedure, apply a small amount of 4% Lidocaine to affected area and allow to dry. Application may be repeated up to 4 times daily.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for this product?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1421893 - lidocaine 4 % Topical Cream
  • RxCUI: 1421893 - lidocaine 40 MG/ML Topical Cream
  • RxCUI: 1876729 - {1 (35000 MG) (lanolin 0.155 MG/MG / petrolatum 0.534 MG/MG Topical Ointment) / 1 (35000 MG) (lidocaine 40 MG/ML Topical Cream) } Pack
  • RxCUI: 1876729 - {1 (35000 MG) (lanolin 15.5 % / petrolatum 53.4 % Topical Ointment)/ 1 (35000 MG) (lidocaine 4 % Topical Cream Topical Cream) } Pack
  • RxCUI: 1876729 - {1 (1.25 OZ) (lanolin 15.5 % / petrolatum 53.4 % Topical Ointment)/ 1 (1.25 OZ) (lidocaine 4 % Topical Cream Topical Cream) } Pack

* Please review the full disclaimer at the bottom of this page.

Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".