Pfa
NDC Package 72119-005-07

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Pfa is put enough product in the palm to cover hands & rub together briskly until the liquid is dryChildren under 6 should be supervised when using Sanitizers. Marketed by Blue Sea Aerosol & Daily Care Co., Ltd, this product is identified by NDC 72119-005 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
72119-005-07
Package Description
100 mL in 1 BOTTLE, PLASTIC
Product Code
72119-005
11-Digit Billing Format
72119000507

Clinical Specifications

Proprietary Name
Pfa
Dosage Form
-
Usage Information
Put enough product in the palm to cover hands & rub together briskly until the liquid is dryChildren under 6 should be supervised when using Sanitizers.

Regulatory & Marketing

Labeler Name
Blue Sea Aerosol & Daily Care Co., Ltd
FDA Application #
part333A
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
06-04-2021
Listing Expiration
12-31-2022
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (72119-005). Click a package code to view its specific billing and regulatory data.

72119-005-01
2 mL in 1 POUCH
72119-005-02
60 mL in 1 BOTTLE, PLASTIC
72119-005-03
500 mL in 1 BOTTLE, PUMP
72119-005-04
237 mL in 1 BOTTLE, PUMP
72119-005-05
375 mL in 1 BOTTLE, PUMP
72119-005-06
80 mL in 1 BOTTLE, PLASTIC

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 72119-005-07 identifies a specific commercial package of 100 ml in 1 bottle, plastic of Pfa, labeled by Blue Sea Aerosol & Daily Care Co., Ltd. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Blue Sea Aerosol & Daily Care Co., Ltd on June 04, 2021. The current certification is valid through December 31, 2022.

How is this Blue Sea Aerosol & Daily Care Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72119000507. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
72119-005-07
11-Digit CMS (5-4-2)
72119-0005-07

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.