73750-459 NDC - DR JS NATURAL 75% ALCOHOL WIPES ()

Drug Information

  • Product NDC: 73750-459
  • Proprietary Name: Dr Js Natural 75% Alcohol Wipes
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Qyk Brands LLC
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:7/1/2020

Package Information

No. Package Code Package Description Billing Unit
173750-459-10100 mL in 1 CANISTER (73750-459-10)
273750-459-211 PACKAGE in 1 PACKET (73750-459-21) / 6 mL in 1 PACKAGE
373750-459-2210 PACKAGE in 1 POUCH (73750-459-22) / 6 mL in 1 PACKAGE
473750-459-2320 PACKAGE in 1 POUCH (73750-459-23) / 6 mL in 1 PACKAGE
573750-459-2430 PACKAGE in 1 POUCH (73750-459-24) / 6 mL in 1 PACKAGE
673750-459-2550 PACKAGE in 1 POUCH (73750-459-25) / 6 mL in 1 PACKAGE
773750-459-2680 PACKAGE in 1 CANISTER (73750-459-26) / 6 mL in 1 PACKAGE
873750-459-27100 PACKAGE in 1 CANISTER (73750-459-27) / 6 mL in 1 PACKAGE
973750-459-28160 PACKAGE in 1 CANISTER (73750-459-28) / 6 mL in 1 PACKAGE
1073750-459-29500 PACKAGE in 1 CANISTER (73750-459-29) / 6 mL in 1 PACKAGE
1173750-459-31700 PACKAGE in 1 CANISTER (73750-459-31) / 6 mL in 1 PACKAGE
1273750-459-40400 PACKAGE in 1 CANISTER (73750-459-40) / 6 mL in 1 PACKAGE

NDC Record

Field Name Field Value Definition
PRODUCT NDC73750-459The 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 NAMEDr Js Natural 75% Alcohol 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 DATE7/1/2020This 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 NAMEQyk Brands LLCName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC73750-459The 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 NAMEDr Js Natural 75% Alcohol 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 DATE7/1/2020This 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 NAMEQyk Brands LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 1/2/2026

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