NDC Package 67618-165-01 Betadine Dry Powder

Povidone-iodine Aerosol, Spray Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

67618-165-01

Package Description:

56.7 mL in 1 CAN

Product Code:

67618-165

Proprietary Name:

Betadine Dry Powder

Non-Proprietary Name:

Povidone-iodine

Substance Name:

Povidone-iodine

Usage Information:

Clean the affected areaSHAKE WELL BEFORE USEHold can approximately 6 inches from wound and apply a thin layer over affected area 1 to 3 dailyMay be covered with a sterile bandage

11-Digit NDC Billing Format:

67618016501

Billing Unit:

GM - Billing unit of "gram" is used when a product is measured by its weight.

NDC to RxNorm Crosswalk:

RxCUI: 153060 - povidone-iodine 0.5 % Powder Spray

RxCUI: 153060 - povidone-iodine 0.005 MG/MG Powder Spray

RxCUI: 2374358 - Betadine 0.5 % Powder Spray

RxCUI: 2374358 - povidone-iodine 0.005 MG/MG Powder Spray [Betadine]

RxCUI: 2374358 - Betadine 0.005 MG/MG Powder Spray

Product Type:

Human Otc Drug

Labeler Name:

Atlantis Consumer Healthcare, Inc.

Dosage Form:

Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.

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 .05 mg/mL

Sample Package:

FDA Application Number:

M003

Marketing Category:

OTC MONOGRAPH DRUG -

Start Marketing Date:

06-15-2020

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

67618 - Atlantis Consumer Healthcare, Inc.
- 67618-165 - Betadine Dry Powder
  - 67618-165-01 - 56.7 mL in 1 CAN

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 67618-165-01?

The NDC Packaged Code 67618-165-01 is assigned to a package of 56.7 ml in 1 can of Betadine Dry Powder, a human over the counter drug labeled by Atlantis Consumer Healthcare, Inc.. The product's dosage form is aerosol, spray and is administered via topical form.

Is NDC 67618-165 included in the NDC Directory?

Yes, Betadine Dry Powder with product code 67618-165 is active and included in the NDC Directory. The product was first marketed by Atlantis Consumer Healthcare, Inc. on June 15, 2020 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 NDC billing unit for package 67618-165-01?

The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight.

What is the 11-digit format for NDC 67618-165-01?

The 11-digit format is 67618016501. 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	67618-165-01	5-4-2	67618-0165-01

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