75209-011 NDC - ZAPRO HAND SANITIZER ()

Drug Information

Product NDC: 75209-011

Proprietary Name: ZAPRO HAND SANITIZER

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: GUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/22/2020

Package Information

No. Package Code Package Description Billing Unit
175209-011-01250 mL in 1 BOTTLE (75209-011-01)
275209-011-022000 mL in 1 BOTTLE (75209-011-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75209-011The 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 NAMEZAPRO HAND SANITIZERThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/22/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGUANGDONG MINGLIU TECHNOLOGY DAIL-USE CHEMICAL CO., LTD.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