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

Lanolin,Petrolatum And Lidocaine Kit - View Dosage, Usage, Ingredients, Routes, UNII

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

NDC Product Code:
67234-047
Proprietary Name:
Skullduggery Pain Relief And Skin Protection For Tattoos
Non-Proprietary Name: [1]
Lanolin, Petrolatum And Lidocaine
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
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.
Start Marketing Date: [9]
06-04-2003
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
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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 which is a human over the counter drug product labeled by Natureplex, Llc. The generic name of Skullduggery Pain Relief And Skin Protection For Tattoos is lanolin, petrolatum and lidocaine. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 67234-047-01 1 kit in 1 carton * 35 g in 1 tube * 35 g in 1 tube. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Skullduggery Pain Relief And Skin Protection For Tattoos?

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 Skullduggery Pain Relief And Skin Protection For Tattoos UNII Codes?

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

Which are Skullduggery Pain Relief And Skin Protection For Tattoos Inactive Ingredients 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 Skullduggery Pain Relief And Skin Protection For Tattoos?

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 disclaimer below.

Product Footnotes

[1] 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.

[3] 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.

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

[6] 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.

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".