NDC 81577-2000 Diabek-100

Hydrogen Peroxide

NDC Product Code 81577-2000

NDC 81577-2000-2

Package Description: 70 g in 1 TUBE

NDC Product Information

Diabek-100 with NDC 81577-2000 is a a human over the counter drug product labeled by Joaquin Armando Cardenas Urquidez. The generic name of Diabek-100 is hydrogen peroxide. The product's dosage form is gel and is administered via topical form.

Labeler Name: Joaquin Armando Cardenas Urquidez

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

Product Type: Human Otc Drug What kind of product is this?
Indicates 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.

Diabek-100 Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • HYDROGEN PEROXIDE .000005 g/g
  • HYPOCHLOROUS ACID .00002 g/g

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • CARBOMER 940 (UNII: 4Q93RCW27E)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Joaquin Armando Cardenas Urquidez
Labeler Code: 81577
FDA Application Number: part333A What is the FDA Application Number?
This 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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product 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 Date: 03-02-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Diabek-100 Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Hypochlorous acidSodium hypochlorite

Inactive Ingredients


Dosage And Administration

Clean the wound with soap and water, apply Diabek-100 antiseptic solution on the wound 3 times a day or as directed by a doctor. If the wound requires covering, place a wet or dry sterile dressing with antiseptic solution as directed by your doctor.

Indications And Usage

Super oxidation antiseptic GelDoes not irritate, does not generate bacterial resistance, for long-term use.Assists in the healing of:Diabetic foot woundsVaricose ulcersSkin lesionsBroad spectrum, effective against fungi, viruses and bacteria.

Purpose Section


Ask A Doctor

Discontinue use in case of hypersensitivity to the components of Diabek-100.

Keep Out Of Reach Of Children


Warnings And Precautions

Discontinue use in case of hypersensitivity to the components of Diabek-100.


Keep in a cool place and away from direct sunlight.

* Please review the disclaimer below.