74757-002 NDC - ALCOHOL-BASED DISINFECTANT HAND SANITIZER ()

Drug Information

  • Product NDC: 74757-002
  • Proprietary Name: ALCOHOL-BASED DISINFECTANT HAND SANITIZER
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: GUIZHOU XINZIHONG PHARMACEUTIC ADJUVANT CO.LTD
Product Type:
FDA Application Number: M005
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:3/20/2020

Package Information

No. Package Code Package Description Billing Unit
174757-002-01100 mL in 1 BOTTLE (74757-002-01)
274757-002-02330 mL in 1 BOTTLE (74757-002-02)
374757-002-03500 mL in 1 BOTTLE (74757-002-03)
474757-002-0460 mL in 1 BOTTLE (74757-002-04)
574757-002-05120 mL in 1 BOTTLE (74757-002-05)
674757-002-06236 mL in 1 BOTTLE (74757-002-06)
774757-002-07250 mL in 1 BOTTLE (74757-002-07)
874757-002-08300 mL in 1 BOTTLE (74757-002-08)
974757-002-091000 mL in 1 BOTTLE (74757-002-09)
1074757-002-102000 mL in 1 BOTTLE (74757-002-10)
1174757-002-113000 mL in 1 BOTTLE (74757-002-11)
1274757-002-124000 mL in 1 BOTTLE (74757-002-12)
1374757-002-135000 mL in 1 BOTTLE (74757-002-13)

NDC Record

Field Name Field Value Definition
PRODUCT NDC74757-002The 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 NAMEALCOHOL-BASED DISINFECTANT 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 DATE3/20/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERM005This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEGUIZHOU XINZIHONG PHARMACEUTIC ADJUVANT CO.LTDName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record record in Text format: Export

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

Download this NDC record record in XML format: Export

This page was last updated on: 12/19/2025

Previous Code
Next Code