NDC 81835-111 R-zero Ethyl Alcohol Antiseptic Hand Sanitizing Fragrance Free

Ethyl Alcohol

NDC Product Code 81835-111

NDC CODE: 81835-111

Proprietary Name: R-zero Ethyl Alcohol Antiseptic Hand Sanitizing Fragrance Free What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Ethyl Alcohol What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 81835 - R-zero Systems, Inc.
    • 81835-111 - R-zero Ethyl Alcohol Antiseptic Hand Sanitizing Fragrance Free

NDC 81835-111-01

Package Description: 1000 mL in 1 BAG

NDC Product Information

R-zero Ethyl Alcohol Antiseptic Hand Sanitizing Fragrance Free with NDC 81835-111 is a a human over the counter drug product labeled by R-zero Systems, Inc.. The generic name of R-zero Ethyl Alcohol Antiseptic Hand Sanitizing Fragrance Free is ethyl alcohol. The product's dosage form is gel and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 581662.

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.

R-zero Ethyl Alcohol Antiseptic Hand Sanitizing Fragrance Free 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.

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.

  • 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: R-zero Systems, Inc.
Labeler Code: 81835
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: 01-01-2022 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.

R-zero Ethyl Alcohol Antiseptic Hand Sanitizing Fragrance Free Product Label Images

R-zero Ethyl Alcohol Antiseptic Hand Sanitizing Fragrance Free 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 Ingredient

Ethyl alcohol 70% v/v




• hand sanitizer to decrease bacteria on the skin• recommended for repeated use• for use when soap and water are not available


Flammable, keep away from fire/flameFor external use onlyDo not use• in children less than 2 months of age• on open skin woundsWhen using this product• do not get into eyes. In case of contact, rinse eyes thoroughly with waterStop use and ask a doctor if• irritation and redness develop• condition persists for more than 72 hours

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


• wet hands thoroughly with product and allow to dry without wiping• rub hands lightly until dry• do not rinse• supervise children under 6 years of age when using this product to avoid swallowing

Other Information

Store below 105˚F (40˚C)

Inactive Ingredients

Acrylates/vinyl isodecanoate crosspolymer, aloe vera (Aloe barbadensis) leaf juice, alpha tocopherol acetate, glycerin, isopropyl myristate, panthenol, peg-6, water (aqua)

Questions? +1-801-823-0314

You may also report serious side effects to this phone number. Mon-Fri 8am - 5pm pst

* Please review the disclaimer below.