NDC 11344-770-34 Germ-x Everywhere
Advanced Hand Sanitizer Gel Topical

Package Information

What is NDC 11344-770-34?

The NDC Code 11344-770-34 is assigned to a package of 236 ml in 1 bottle, pump of Germ-x Everywhere, a human over the counter drug labeled by Vi Jon, Llc. The product's dosage form is gel and is administered via topical form. The following table has all the important details about this NDC code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

Field Name Field Value
NDC Code 11344-770-34
Package Description 236 mL in 1 BOTTLE, PUMP
Product Code 11344-770
Proprietary Name 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.
Germ-x Everywhere
Non-Proprietary Name 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.
Advanced Hand Sanitizer
Usage Information Product Usage Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
This product is used as Antiseptic. To decrease bacteria on the skin that could cause diseaserecommend for repeated use
11-Digit NDC Billing Format NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
NDC to RxNorm Crosswalk
  • RxCUI: 581662 - ethanol 70 % Topical Gel
  • RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
  • RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
  • Product Type 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.
    Human Otc Drug
    Labeler Name Vi Jon, Llc
    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.
    Administration Route(s)
    • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    Active Ingredient(s)
    Sample Package Sample Package?
    This field Indicates whether this package is a sample packaging or not.
    Marketing Category 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.
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    FDA Application Number 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.
    Start Marketing Date 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 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 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".
    NDC Code Structure

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for Germ-x Everywhere with product NDC 11344-770.

    NDC Package CodePackage Description
    11344-770-04750 mL in 1 BOTTLE, PLASTIC
    11344-770-083785 mL in 1 BOTTLE, PLASTIC
    11344-770-1659 mL in 1 BOTTLE, PLASTIC
    11344-770-26118 mL in 1 BOTTLE, PLASTIC
    11344-770-271150 mL in 1 BOTTLE, PLASTIC
    11344-770-32355 mL in 1 BOTTLE, PLASTIC
    11344-770-38295 mL in 1 BOTTLE, PLASTIC
    11344-770-45946 mL in 1 BOTTLE, PLASTIC
    11344-770-49443 mL in 1 BOTTLE, PLASTIC
    11344-770-861000 mL in 1 BOTTLE, PLASTIC
    11344-770-881999 mL in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.