75757-128 NDC - CYBER CLEAN MOISTURIZING HAND SANITIZERSPRAY EUCALYPTUS ()

Drug Information

  • Product NDC: 75757-128
  • Proprietary Name: Cyber Clean Moisturizing Hand SanitizerSpray Eucalyptus
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: JOKER AG
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:11/2/2020

Package Information

No. Package Code Package Description Billing Unit
175757-128-0150 mL in 1 BOTTLE (75757-128-01)
275757-128-02100 mL in 1 BOTTLE (75757-128-02)
375757-128-03175 mL in 1 BOTTLE (75757-128-03)
475757-128-04250 mL in 1 BOTTLE (75757-128-04)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75757-128The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
PROPRIETARY NAMECyber Clean Moisturizing Hand SanitizerSpray EucalyptusIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
START MARKETING DATE11/2/2020The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
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 NAMEJOKER AGAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

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This page was last updated on: 12/19/2025

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