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  5. NDC Package Code: 67234-066-01 Tattoo After Care A And D

NDC Package 67234-066-01 Tattoo After Care A And D

Lanolin And Petrolatum Ointment Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
67234-066-01
Package Description:
1 TUBE in 1 CARTON / 42.5 g in 1 TUBE
Product Code:
67234-066
Proprietary Name:
Tattoo After Care A And D
Non-Proprietary Name:
Lanolin And Petrolatum
Substance Name:
Lanolin; Petrolatum
Usage Information:
This product is used as Active ingredientsPurposeLanolin 15.5%Skin protectantPetrolatum 53.4%Skin protectant. Temporarily protects minor:cutsscrapesburnstemporarily protects chapped or cracked skin and lips
11-Digit NDC Billing Format:
67234006601
NDC to RxNorm Crosswalk:
  • RxCUI: 664981 - lanolin 15.5 % / petrolatum 53.4 % Topical Ointment
  • RxCUI: 664981 - lanolin 0.155 MG/MG / petrolatum 0.534 MG/MG Topical Ointment
  • RxCUI: 664981 - lanolin 15.5 GM per 100 GM / petrolatum 53.4 GM per 100 GM Topical Ointment
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Natureplex Llc
    Dosage Form:
    Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • LANOLIN .15 mg/g
  • PETROLATUM .53 mg/g
    • Sample Package:
    No
    FDA Application Number:
    part347
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    06-15-2018
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 67234-066-01?

    The NDC Packaged Code 67234-066-01 is assigned to a package of 1 tube in 1 carton / 42.5 g in 1 tube of Tattoo After Care A And D, a human over the counter drug labeled by Natureplex Llc. The product's dosage form is ointment and is administered via topical form.

    Is NDC 67234-066 included in the NDC Directory?

    Yes, Tattoo After Care A And D with product code 67234-066 is active and included in the NDC Directory. The product was first marketed by Natureplex Llc on June 15, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 67234-066-01?

    The 11-digit format is 67234006601. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-267234-066-015-4-267234-0066-01