NDC Package 0395-9136-23 Povidone Iodine

Povidone Iodine Oral Rinse 0.5% Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information
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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:

0395-9136-23

Package Description:

20 mL in 1 CONTAINER

Product Code:

0395-9136

Proprietary Name:

Povidone Iodine

Non-Proprietary Name:

Povidone Iodine Oral Rinse 0.5%

Substance Name:

Povidone-iodine

Usage Information:

Use full strength.Apply 10 to 20 milliliters of solution to the operative site. Instruct the patient to rinse for 30 seconds and then spit out.Wait 2 minutes, and apply another 10 to 20 milliliters of solution to the operative site. Instruct the patient to rinse again for 30 seconds and then spit out.With a standard syringe and a blunt, angulated needle, irrigate the operative site and the surrounding gingival mucosa for 1 minute with 10 to 20 milliliters of the solution. Instruct the patient to spit out the solution after the irrigation procedure.

11-Digit NDC Billing Format:

00395913623

NDC to RxNorm Crosswalk:

RxCUI: 314935 - povidone-iodine 0.5 % Mouthwash

RxCUI: 314935 - povidone-iodine 5 MG/ML Mouthwash

Product Type:

Human Otc Drug

Labeler Name:

Humco Holding Group, Inc.

Dosage Form:

Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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):

POVIDONE-IODINE 5 mg/mL

Sample Package:

FDA Application Number:

M022

Marketing Category:

OTC MONOGRAPH DRUG -

Start Marketing Date:

01-06-2021

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

0395 - Humco Holding Group, Inc.
- 0395-9136 - Povidone Iodine
  - 0395-9136-23 - 20 mL in 1 CONTAINER

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.

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Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
0395-9136-98	237 mL in 1 CONTAINER

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Frequently Asked Questions

What is NDC 0395-9136-23?

The NDC Packaged Code 0395-9136-23 is assigned to a package of 20 ml in 1 container of Povidone Iodine, a human over the counter drug labeled by Humco Holding Group, Inc.. The product's dosage form is liquid and is administered via topical form.

Is NDC 0395-9136 included in the NDC Directory?

Yes, Povidone Iodine with product code 0395-9136 is active and included in the NDC Directory. The product was first marketed by Humco Holding Group, Inc. on January 06, 2021 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 0395-9136-23?

The 11-digit format is 00395913623. 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 4-4-2 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
4-4-2	0395-9136-23	5-4-2	00395-9136-23

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