78536-001 NDC - DISINFECTANT WIPES ()

Drug Information

  • Product NDC: 78536-001
  • Proprietary Name: Disinfectant Wipes
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Zhejiang Yiwu Mingou Biotechnology Co., Ltd.
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:6/5/2020

Package Information

No. Package Code Package Description Billing Unit
178536-001-01180 BAG in 1 CARTON (78536-001-01) / 10 POUCH in 1 BAG / 50 mL in 1 POUCH
278536-001-02120 BAG in 1 CARTON (78536-001-02) / 15 POUCH in 1 BAG / 75 mL in 1 POUCH
378536-001-0390 BAG in 1 CARTON (78536-001-03) / 20 POUCH in 1 BAG / 100 mL in 1 POUCH
478536-001-0472 BAG in 1 CARTON (78536-001-04) / 25 POUCH in 1 BAG / 125 mL in 1 POUCH
578536-001-0560 BAG in 1 CARTON (78536-001-05) / 30 POUCH in 1 BAG / 150 mL in 1 POUCH
678536-001-0636 BAG in 1 CARTON (78536-001-06) / 40 POUCH in 1 BAG / 200 mL in 1 POUCH
778536-001-0730 BAG in 1 CARTON (78536-001-07) / 54 POUCH in 1 BAG / 220 mL in 1 POUCH
878536-001-0824 BAG in 1 CARTON (78536-001-08) / 72 POUCH in 1 BAG / 360 mL in 1 POUCH
978536-001-0924 BAG in 1 CARTON (78536-001-09) / 80 POUCH in 1 BAG / 400 mL in 1 POUCH
1078536-001-1024 BAG in 1 CARTON (78536-001-10) / 100 POUCH in 1 BAG / 5000 mL in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC78536-001The 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 NAMEDisinfectant 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 DATE6/5/2020This 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 NAMEZhejiang Yiwu Mingou Biotechnology 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: 12/19/2025

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