St. Ives Blemish And Blackhead Control
NDC Package 54726-0100-9

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.

St. Ives Blemish And Blackhead Control is moisten face with water. Marketed by Cosmetic Laboratories Of America, this product is identified by NDC 54726-0100 and is authorized under FDA application part333D.

Identification & Billing

NDC Package Code
54726-0100-9
Package Description
283 g in 1 TUBE
Product Code
54726-0100
11-Digit Billing Format
54726010009
RxNorm Crosswalk
  • RxCUI: 1039716 - St. Ives 2 % Medicated Liquid Soap
  • RxCUI: 1039716 - salicylic acid 20 MG/ML Medicated Liquid Soap [St. Ives Blemish & Blackhead Control]
  • RxCUI: 1039716 - St. Ives Blemish & Blackhead Control 2 % Medicated Liquid Soap
  • RxCUI: 1039716 - St. Ives Blemish & Blackhead Control 20 MG/ML Medicated Liquid Soap
  • RxCUI: 1039716 - St. Ives Green Tea 2 % Medicated Liquid Soap

Clinical Specifications

Proprietary Name
St. Ives Blemish And Blackhead Control
Dosage Form
-
Usage Information
Moisten face with water. Dispense product onto fingertips and massage over face. Rinse with water. Avoid direct contact with eyes. In case of contact with eyes, flush thoroughly with water. For best results use 3 to 4 times per week.

Regulatory & Marketing

Labeler Name
Cosmetic Laboratories Of America
FDA Application #
part333D
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
02-23-2011
Listing Expiration
12-31-2017
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 (54726-0100). Click a package code to view its specific billing and regulatory data.

54726-0100-1
28 g in 1 TUBE
54726-0100-3
3 TUBE in 1 CARTON / 212 g in 1 TUBE
54726-0100-6
170 g in 1 TUBE
54726-0100-7
212 g in 1 TUBE

* 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 54726-0100-9 identifies a specific commercial package of 283 g in 1 tube of St. Ives Blemish And Blackhead Control, labeled by Cosmetic Laboratories Of America. 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 Cosmetic Laboratories Of America on February 23, 2011. The current certification is valid through December 31, 2017.

How is this Cosmetic Laboratories Of America product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 54726010009. 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 (5-4-1)
54726-0100-9
11-Digit CMS (5-4-2)
54726-0100-09

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