Venrock Spray
NDC Package 85772-0002-1

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

Package Information

Venrock (piroctone olamine and salicylic acid) sprays is shake well before useApply to affected areas one to four times daily or as directed by a doctorFor best results, use at least twice a week or as directed by a doctorApplication: Hold 15-20 cm (4-6 inches) from dry scalp and spray onto affected areas. This formulation utilizes a spray delivery system. Marketed by Guangzhou Oupeng Cosmetics Co., Ltd., this product is identified by NDC 85772-0002 and is authorized under FDA application M032.

Identification & Billing

NDC Package Code
85772-0002-1
Package Description
1 g in 1 BOX
Product Code
85772-0002
11-Digit Billing Format
85772000201
RxNorm Crosswalk
  • RxCUI: 2717186 - piroctone olamine 0.5 % / salicylic acid 1.5 % Topical Spray
  • RxCUI: 2717186 - piroctone olamine 5 MG/ML / salicylic acid 15 MG/ML Topical Spray

Clinical Specifications

Proprietary Name
Venrock
Non-Proprietary Name
Piroctone Olamine And Salicylic Acid
Substance Name
Piroctone Olamine; Salicylic Acid
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
  • Cutaneous - Administration to the skin.
  • 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)
Usage Information
Shake well before useApply to affected areas one to four times daily or as directed by a doctorFor best results, use at least twice a week or as directed by a doctorApplication: Hold 15-20 cm (4-6 inches) from dry scalp and spray onto affected areas. Use fingertips to massage into scalp for 1-2 minutes until fully absorbed. Do not rinse.

Regulatory & Marketing

Labeler Name
Guangzhou Oupeng Cosmetics Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M032
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-20-2025
Listing Expiration
12-31-2026
Exclude Flag
N
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 85772-0002-1 identifies a specific commercial package of 1 g in 1 box of Venrock, a human over the counter drug labeled by Guangzhou Oupeng Cosmetics Co., Ltd.. This spray is formulated for cutaneous; topical use and contains piroctone olamine; salicylic acid as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Guangzhou Oupeng Cosmetics Co., Ltd. on June 20, 2025. The current certification is valid through December 31, 2026.

How is this Guangzhou Oupeng Cosmetics Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85772000201. 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)
85772-0002-1
11-Digit CMS (5-4-2)
85772-0002-01

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