80707-101 NDC - DISINFECTING WIPES ()

Drug Information

  • Product NDC: 80707-101
  • Proprietary Name: DISINFECTING WIPES
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Hangzhou Muzi Commodity Co., Ltd
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/30/2020
End Marketing Date:12/17/2020

Package Information

No. Package Code Package Description Billing Unit
180707-101-0135 SOLUTION in 1 BOTTLE (80707-101-01)
280707-101-0240 SOLUTION in 1 BOTTLE (80707-101-02)
380707-101-0350 SOLUTION in 1 BOTTLE (80707-101-03)
480707-101-0460 SOLUTION in 1 BOTTLE (80707-101-04)
580707-101-0570 SOLUTION in 1 BOTTLE (80707-101-05)
680707-101-0675 SOLUTION in 1 BOTTLE (80707-101-06)
780707-101-0780 SOLUTION in 1 BOTTLE (80707-101-07)
880707-101-0890 SOLUTION in 1 BOTTLE (80707-101-08)
980707-101-09100 SOLUTION in 1 BOTTLE (80707-101-09)
1080707-101-10120 SOLUTION in 1 BOTTLE (80707-101-10)
1180707-101-11150 SOLUTION in 1 BOTTLE (80707-101-11)
1280707-101-12160 SOLUTION in 1 BOTTLE (80707-101-12)
1380707-101-13180 SOLUTION in 1 BOTTLE (80707-101-13)
1480707-101-14200 SOLUTION in 1 BOTTLE (80707-101-14)
1580707-101-15250 SOLUTION in 1 BOTTLE (80707-101-15)
1680707-101-16300 SOLUTION in 1 BOTTLE (80707-101-16)

NDC Record

Field Name Field Value Definition
PRODUCT NDC80707-101The 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 NAMEDISINFECTING WIPESThe 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 DATE12/17/2020This 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 NOT FINALProduct 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 NUMBERpart333AThis 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 NAMEHangzhou Muzi Commodity Co., LtdName of Company corresponding to the labeler code segment of the Product NDC.

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

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