78410-001 NDC - DISNFECTING WIPES ()

Drug Information

  • Product NDC: 78410-001
  • Proprietary Name: Disnfecting Wipes
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Wenzhou Mingwei Paper Co., Ltd.
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:6/9/2020

Package Information

No. Package Code Package Description Billing Unit
178410-001-0148 POUCH in 1 PAIL (78410-001-01) / 225 g in 1 POUCH
278410-001-0248 PAIL in 1 CARTON (78410-001-02) / 70 POUCH in 1 PAIL / 250 g in 1 POUCH
378410-001-0348 PAIL in 1 CARTON (78410-001-03) / 100 POUCH in 1 PAIL / 300 g in 1 POUCH
478410-001-04100 BAG in 1 CARTON (78410-001-04) / 30 POUCH in 1 BAG / 150 g in 1 POUCH
578410-001-0524 BAG in 1 CARTON (78410-001-05) / 40 POUCH in 1 BAG / 220 g in 1 POUCH
678410-001-0648 PAIL in 1 CARTON (78410-001-06) / 60 POUCH in 1 PAIL / 200 g in 1 POUCH
778410-001-0724 PAIL in 1 CARTON (78410-001-07) / 100 POUCH in 1 PAIL / 350 g in 1 POUCH
878410-001-0824 PAIL in 1 CARTON (78410-001-08) / 160 POUCH in 1 PAIL / 450 g in 1 POUCH
978410-001-0912 PAIL in 1 CARTON (78410-001-09) / 200 POUCH in 1 PAIL / 600 g in 1 POUCH
1078410-001-104 PAIL in 1 CARTON (78410-001-10) / 500 POUCH in 1 PAIL / 1500 g in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC78410-001The 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 NAMEDisnfecting 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 DATE6/9/2020This 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 NAMEWenzhou Mingwei Paper 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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