80707-201 NDC - DISINFECTING WIPES ()

Drug Information

  • Product NDC: 80707-201
  • 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

Package Information

No. Package Code Package Description Billing Unit
180707-201-0135 CLOTH in 1 BOTTLE (80707-201-01)
280707-201-0240 CLOTH in 1 BOTTLE (80707-201-02)
380707-201-0350 CLOTH in 1 BOTTLE (80707-201-03)
480707-201-0460 CLOTH in 1 BOTTLE (80707-201-04)
580707-201-0570 CLOTH in 1 BOTTLE (80707-201-05)
680707-201-0675 CLOTH in 1 BOTTLE (80707-201-06)
780707-201-0780 CLOTH in 1 BOTTLE (80707-201-07)
880707-201-0890 CLOTH in 1 BOTTLE (80707-201-08)
980707-201-09100 CLOTH in 1 BOTTLE (80707-201-09)
1080707-201-10120 CLOTH in 1 BOTTLE (80707-201-10)
1180707-201-11150 CLOTH in 1 BOTTLE (80707-201-11)
1280707-201-12160 CLOTH in 1 BOTTLE (80707-201-12)
1380707-201-13180 CLOTH in 1 BOTTLE (80707-201-13)
1480707-201-14200 CLOTH in 1 BOTTLE (80707-201-14)
1580707-201-15250 CLOTH in 1 BOTTLE (80707-201-15)
1680707-201-16300 CLOTH in 1 BOTTLE (80707-201-16)

NDC Record

Field Name Field Value Definition
PRODUCT NDC80707-201The 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 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.
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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