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  5. NDC Package Code: 71262-009-01 Tetracyte Topical Tetracycline Hydrochloride

NDC Package 71262-009-01 Tetracyte Topical Tetracycline Hydrochloride

Tetracycline Hydrochloride 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:
71262-009-01
Package Description:
1 BOTTLE in 1 CARTON / 15 mL in 1 BOTTLE
Product Code:
71262-009
Proprietary Name:
Tetracyte Topical Tetracycline Hydrochloride
Non-Proprietary Name:
Tetracycline Hydrochloride
Substance Name:
Tetracycline Hydrochloride
Usage Information:
First aid to help prevent the risk of skin infection in minor cuts, scrapes, or burns.
11-Digit NDC Billing Format:
71262000901
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Viaderma Distribution Inc
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):
TETRACYCLINE HYDROCHLORIDE 30 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M004
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
05-01-2024
Listing Expiration Date:
12-31-2025
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 71262-009-01?

The NDC Packaged Code 71262-009-01 is assigned to a package of 1 bottle in 1 carton / 15 ml in 1 bottle of Tetracyte Topical Tetracycline Hydrochloride, a human over the counter drug labeled by Viaderma Distribution Inc. The product's dosage form is ointment and is administered via topical form.

Is NDC 71262-009 included in the NDC Directory?

Yes, Tetracyte Topical Tetracycline Hydrochloride with product code 71262-009 is active and included in the NDC Directory. The product was first marketed by Viaderma Distribution Inc on May 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71262-009-01?

The 11-digit format is 71262000901. 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
5-3-271262-009-015-4-271262-0009-01