42851-084 NDC - ZO MEDICAL SURFATROL ASTRINGENT ()

Drug Information

Product NDC: 42851-084

Proprietary Name: ZO MEDICAL SURFATROL Astringent

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ZO Skin Health, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/1/2016

Package Information

No. Package Code Package Description Billing Unit
142851-084-1910 PACKET in 1 CARTON (42851-084-19) / 6 g in 1 PACKET

NDC Record

Field Name Field Value Definition
PRODUCT NDC42851-084The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEZO MEDICAL SURFATROL AstringentThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/1/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEZO Skin Health, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023