79539-201 NDC - INSTANT HAND SANITIZEING WIPE ()

Drug Information

  • Product NDC: 79539-201
  • Proprietary Name: Instant Hand Sanitizeing Wipe
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Shandong Yayun Sanitary Products Co., Ltd.
Product Type:
FDA Application Number: M003
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:3/30/2020
End Marketing Date:11/21/2024

Package Information

No. Package Code Package Description Billing Unit
179539-201-0110 CLOTH in 1 BAG (79539-201-01)
279539-201-0220 CLOTH in 1 BAG (79539-201-02)
379539-201-0330 CLOTH in 1 BAG (79539-201-03)
479539-201-0440 CLOTH in 1 BAG (79539-201-04)
579539-201-0550 CLOTH in 1 BAG (79539-201-05)
679539-201-0660 CLOTH in 1 BAG (79539-201-06)
779539-201-0770 CLOTH in 1 BAG (79539-201-07)
879539-201-0880 CLOTH in 1 BAG (79539-201-08)
979539-201-09100 CLOTH in 1 BAG (79539-201-09)
1079539-201-10120 CLOTH in 1 BAG (79539-201-10)
1179539-201-11150 CLOTH in 1 BAG (79539-201-11)
1279539-201-12160 CLOTH in 1 BAG (79539-201-12)
1379539-201-13180 CLOTH in 1 BAG (79539-201-13)
1479539-201-14200 CLOTH in 1 BAG (79539-201-14)
1579539-201-15300 CLOTH in 1 BAG (79539-201-15)
1679539-201-16400 CLOTH in 1 BAG (79539-201-16)
1779539-201-17500 CLOTH in 1 BAG (79539-201-17)
1879539-201-18600 CLOTH in 1 BAG (79539-201-18)
1979539-201-19700 CLOTH in 1 BAG (79539-201-19)
2079539-201-20800 CLOTH in 1 BAG (79539-201-20)
2179539-201-211000 CLOTH in 1 BAG (79539-201-21)
2279539-201-221200 CLOTH in 1 BAG (79539-201-22)
2379539-201-231600 CLOTH in 1 BAG (79539-201-23)
2479539-201-242000 CLOTH in 1 BAG (79539-201-24)

NDC Record

Field Name Field Value Definition
PRODUCT NDC79539-201The 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 NAMEInstant Hand Sanitizeing WipeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/30/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE11/21/2024This 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 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 NUMBERM003This 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 NAMEShandong Yayun Sanitary Products Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/4/2025

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