NDC Package 85772-0002-1 Venrock

Piroctone Olamine And Salicylic Acid Spray Cutaneous; Topical - View Billable Units, 11-Digit Format, RxNorm

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:
85772-0002-1
Package Description:
1 g in 1 BOX
Product Code:
Proprietary Name:
Venrock
Non-Proprietary Name:
Piroctone Olamine And Salicylic Acid
Substance Name:
Piroctone Olamine; Salicylic Acid
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.
11-Digit NDC Billing Format:
85772000201
NDC to 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
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Oupeng Cosmetics Co., Ltd.
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s):
  • 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.
Sample Package:
No
FDA Application Number:
M032
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
06-20-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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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Frequently Asked Questions

What is NDC 85772-0002-1?

The NDC Packaged Code 85772-0002-1 is assigned to a package of 1 g in 1 box of Venrock, a human over the counter drug labeled by Guangzhou Oupeng Cosmetics Co., Ltd.. The product's dosage form is spray and is administered via cutaneous; topical form.

Is NDC 85772-0002 included in the NDC Directory?

Yes, Venrock with product code 85772-0002 is active and included in the NDC Directory. The product was first marketed by Guangzhou Oupeng Cosmetics Co., Ltd. on June 20, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 85772-0002-1?

The 11-digit format is 85772000201. 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 5-4-1 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-185772-0002-15-4-285772-0002-01