74046-002 NDC - HAND SANITIZER ()

Drug Information

  • Product NDC: 74046-002
  • Proprietary Name: HAND SANITIZER
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Dongguan Mingyi Medical Products Co., Ltd.
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:4/14/2020
End Marketing Date:1/14/2022

Package Information

No. Package Code Package Description Billing Unit
174046-002-013 mL in 1 BOTTLE (74046-002-01)
274046-002-0210 mL in 1 BOTTLE (74046-002-02)
374046-002-0315 mL in 1 BOTTLE (74046-002-03)
474046-002-0420 mL in 1 BOTTLE (74046-002-04)
574046-002-0530 mL in 1 BOTTLE (74046-002-05)
674046-002-0638 mL in 1 BOTTLE (74046-002-06)
774046-002-0740 mL in 1 BOTTLE (74046-002-07)
874046-002-0845 mL in 1 BOTTLE (74046-002-08)
974046-002-0950 mL in 1 BOTTLE (74046-002-09)
1074046-002-1060 mL in 1 BOTTLE (74046-002-10)
1174046-002-1170 mL in 1 BOTTLE (74046-002-11)
1274046-002-1280 mL in 1 BOTTLE (74046-002-12)
1374046-002-13100 mL in 1 BOTTLE (74046-002-13)
1474046-002-14120 mL in 1 BOTTLE (74046-002-14)
1574046-002-15236 mL in 1 BOTTLE (74046-002-15)
1674046-002-16240 mL in 1 BOTTLE (74046-002-16)
1774046-002-17250 mL in 1 BOTTLE (74046-002-17)
1874046-002-18300 mL in 1 BOTTLE (74046-002-18)
1974046-002-19450 mL in 1 BOTTLE (74046-002-19)
2074046-002-20500 mL in 1 BOTTLE (74046-002-20)

NDC Record

Field Name Field Value Definition
PRODUCT NDC74046-002The 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 NAMEHAND 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 DATE4/14/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE1/14/2022This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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.
LABELER NAMEDongguan Mingyi Medical Products Co., Ltd.Name 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: 12/6/2025

Previous Code
Next Code