NDC Package 69396-021-01 Zinc Oxide 20%

Zinc Oxide Ointment Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
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:

69396-021-01

Package Description:

1 TUBE in 1 BOX / 28 g in 1 TUBE

Product Code:

69396-021

Proprietary Name:

Zinc Oxide 20%

Non-Proprietary Name:

Zinc Oxide

Substance Name:

Zinc Oxide

Usage Information:

This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.

11-Digit NDC Billing Format:

69396002101

NDC to RxNorm Crosswalk:

RxCUI: 198911 - zinc oxide 20 % Topical Ointment

RxCUI: 198911 - zinc oxide 0.2 MG/MG Topical Ointment

RxCUI: 198911 - zinc oxide 200 MG per GM Topical Ointment

RxCUI: 198911 - ZNO 0.2 MG/MG Topical Ointment

Product Type:

Human Otc Drug

Labeler Name:

Trifecta Pharmaceuticals Usa

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):

ZINC OXIDE .2 g/g

Sample Package:

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:

01-26-2018

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

69396 - Trifecta Pharmaceuticals Usa
- 69396-021 - Zinc Oxide 20%
  - 69396-021-01 - 1 TUBE in 1 BOX / 28 g in 1 TUBE

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.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
69396-021-02	1 TUBE in 1 BOX / 60 g in 1 TUBE
69396-021-54	1 JAR in 1 JAR / 454 g in 1 JAR

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 69396-021-01?

The NDC Packaged Code 69396-021-01 is assigned to a package of 1 tube in 1 box / 28 g in 1 tube of Zinc Oxide 20%, a human over the counter drug labeled by Trifecta Pharmaceuticals Usa. The product's dosage form is ointment and is administered via topical form.

Is NDC 69396-021 included in the NDC Directory?

Yes, Zinc Oxide 20% with product code 69396-021 is active and included in the NDC Directory. The product was first marketed by Trifecta Pharmaceuticals Usa on January 26, 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 69396-021-01?

The 11-digit format is 69396002101. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	69396-021-01	5-4-2	69396-0021-01

Table of Contents