78411-002 NDC - DEFENDER WIPE ()

Drug Information

  • Product NDC: 78411-002
  • Proprietary Name: Defender Wipe
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Zhejiang Qirun Daily Necessities Co., Ltd.
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:5/30/2020

Package Information

No. Package Code Package Description Billing Unit
178411-002-0110 POUCH in 1 BAG (78411-002-01) / .005265 g in 1 POUCH
278411-002-02900 POUCH in 1 BAG (78411-002-02) / 4.7385 g in 1 POUCH
378411-002-031200 POUCH in 1 BAG (78411-002-03) / 6.318 g in 1 POUCH
478411-002-04180 POUCH in 1 BAG (78411-002-04) / .09477 g in 1 POUCH
578411-002-05250 POUCH in 1 BAG (78411-002-05) / .131625 g in 1 POUCH
678411-002-0680 POUCH in 1 BAG (78411-002-06) / .04212 g in 1 POUCH
778411-002-07800 POUCH in 1 BAG (78411-002-07) / .4212 g in 1 POUCH
878411-002-08180 POUCH in 1 PAIL (78411-002-08) / .09477 g in 1 POUCH
978411-002-09250 POUCH in 1 PAIL (78411-002-09) / 1.31625 g in 1 POUCH
1078411-002-1020 POUCH in 1 BAG (78411-002-10) / .01053 g in 1 POUCH
1178411-002-1150 POUCH in 1 PAIL (78411-002-11) / .01053 g in 1 POUCH
1278411-002-1260 POUCH in 1 PAIL (78411-002-12) / .01053 g in 1 POUCH
1378411-002-1370 POUCH in 1 PAIL (78411-002-13) / .01053 g in 1 POUCH
1478411-002-1480 POUCH in 1 PAIL (78411-002-14) / .01053 g in 1 POUCH
1578411-002-1590 POUCH in 1 PAIL (78411-002-15) / .01053 g in 1 POUCH
1678411-002-16100 POUCH in 1 PAIL (78411-002-16) / .01053 g in 1 POUCH
1778411-002-17160 POUCH in 1 PAIL (78411-002-17) / .01053 g in 1 POUCH
1878411-002-18140 POUCH in 1 PAIL (78411-002-18) / .01053 g in 1 POUCH
1978411-002-19300 POUCH in 1 PAIL (78411-002-19) / .01053 g in 1 POUCH
2078411-002-20500 POUCH in 1 PAIL (78411-002-20) / .01053 g in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC78411-002The 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 NAMEDefender 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 DATE5/30/2020This 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 NAMEZhejiang Qirun Daily Necessities 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: 4/4/2025

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