69821-002 NDC - WET WIPES ()

Drug Information

  • Product NDC: 69821-002
  • Proprietary Name: Wet Wipes
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Zhejiang Qimei Commodity Co.,Ltd.
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:4/20/2020

Package Information

No. Package Code Package Description Billing Unit
169821-002-011 POUCH in 1 PACKAGE (69821-002-01) / 3 g in 1 POUCH
269821-002-0210 POUCH in 1 PACKAGE (69821-002-02) / 3 g in 1 POUCH
369821-002-0315 POUCH in 1 PACKAGE (69821-002-03) / 3 g in 1 POUCH
469821-002-0420 POUCH in 1 PACKAGE (69821-002-04) / 3 g in 1 POUCH
569821-002-0550 POUCH in 1 PACKAGE (69821-002-05) / 3 g in 1 POUCH
669821-002-0660 POUCH in 1 PACKAGE (69821-002-06) / 3 g in 1 POUCH
769821-002-0780 POUCH in 1 PACKAGE (69821-002-07) / 3 g in 1 POUCH
869821-002-08600 POUCH in 1 PACKAGE (69821-002-08) / 3 g in 1 POUCH
969821-002-0950 POUCH in 1 PAIL (69821-002-09) / 1.7 g in 1 POUCH
1069821-002-10160 POUCH in 1 PAIL (69821-002-10) / 1.7 g in 1 POUCH
1169821-002-11250 POUCH in 1 PAIL (69821-002-11) / 1.7 g in 1 POUCH
1269821-002-12600 POUCH in 1 PAIL (69821-002-12) / 1.7 g in 1 POUCH
1369821-002-131200 POUCH in 1 BAG (69821-002-13) / 1.7 g in 1 POUCH
1469821-002-14150 POUCH in 1 PAIL (69821-002-14) / 1.7 g in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC69821-002The 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 NAMEWet 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 DATE4/20/2020This 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 Qimei Commodity 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: 2/5/2026

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