52489-521 NDC - SANITIZING WIPES ()

Drug Information

  • Product NDC: 52489-521
  • Proprietary Name: Sanitizing Wipes
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Imperial Palace Commodity (Shenzhen) Co., Ltd
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:9/16/2020

Package Information

No. Package Code Package Description Billing Unit
152489-521-01250 NOT APPLICABLE in 1 CANISTER (52489-521-01) / 250 mL in 1 NOT APPLICABLE
252489-521-02250 NOT APPLICABLE in 1 BAG (52489-521-02) / 250 mL in 1 NOT APPLICABLE
352489-521-0360 NOT APPLICABLE in 1 POUCH (52489-521-03) / 60 mL in 1 NOT APPLICABLE
452489-521-0430 NOT APPLICABLE in 1 POUCH (52489-521-04) / 30 mL in 1 NOT APPLICABLE
552489-521-05800 NOT APPLICABLE in 1 CANISTER (52489-521-05) / 800 mL in 1 NOT APPLICABLE
652489-521-06800 NOT APPLICABLE in 1 BAG (52489-521-06) / 800 mL in 1 NOT APPLICABLE
752489-521-0780 NOT APPLICABLE in 1 BAG (52489-521-07) / 80 mL in 1 NOT APPLICABLE
852489-521-0880 NOT APPLICABLE in 1 CANISTER (52489-521-08) / 80 mL in 1 NOT APPLICABLE
952489-521-09100 NOT APPLICABLE in 1 BAG (52489-521-09) / 100 mL in 1 NOT APPLICABLE
1052489-521-10100 NOT APPLICABLE in 1 CANISTER (52489-521-10) / 100 mL in 1 NOT APPLICABLE
1152489-521-11120 NOT APPLICABLE in 1 BAG (52489-521-11) / 120 mL in 1 NOT APPLICABLE
1252489-521-22120 NOT APPLICABLE in 1 CANISTER (52489-521-22) / 120 mL in 1 NOT APPLICABLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC52489-521The 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 NAMESanitizing 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 DATE9/16/2020This 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 NAMEImperial Palace Commodity (Shenzhen) 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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