53329-211 NDC - EPI-CLENZ INSTANT HAND ANTISEPTIC ()

Drug Information

  • Product NDC: 53329-211
  • Proprietary Name: Epi-Clenz Instant Hand Antiseptic
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Medline Industries, LP
Product Type:
FDA Application Number: part356
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:9/20/2007
End Marketing Date:4/30/2021

Package Information

No. Package Code Package Description Billing Unit
153329-211-06473 mL in 1 BOTTLE, PUMP (53329-211-06)

NDC Record

Field Name Field Value Definition
PRODUCT NDC53329-211The translation of the route code submitted by the firm, indicating route of administration.
PROPRIETARY NAMEEpi-Clenz Instant Hand AntisepticProduct 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.
START MARKETING DATE9/20/2007Name of Company corresponding to the labeler code segment of the Product NDC.
END MARKETING DATE4/30/2021 
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 NUMBERpart356This 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 NAMEMedline Industries, LPName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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