NDC 72772-101 Rebel Green Hand Sanitizer Peppermint And Lemon

Alcohol

NDC Product Code 72772-101

NDC Code: 72772-101

Proprietary Name: Rebel Green Hand Sanitizer Peppermint And Lemon Additional informationCallout TooltipWhat 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: Alcohol Additional informationCallout TooltipWhat 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.


Code Structure
  • 72772 - Rebel Green Llc
    • 72772-101 - Rebel Green Hand Sanitizer

NDC 72772-101-11

Package Description: 500 mL in 1 BOTTLE

NDC 72772-101-12

Package Description: 1005 mL in 1 BOTTLE

NDC Product Information

Rebel Green Hand Sanitizer Peppermint And Lemon with NDC 72772-101 is a a human over the counter drug product labeled by Rebel Green Llc. The generic name of Rebel Green Hand Sanitizer Peppermint And Lemon is alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Rebel Green 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.

Product Type: Human Otc Drug Additional informationCallout TooltipWhat 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.


Rebel Green Hand Sanitizer Peppermint And Lemon Active Ingredient(s)

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

  • ALCOHOL 70 mL/100mL

Inactive Ingredient(s)

Additional informationCallout TooltipAbout 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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
  • AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
  • PEPPERMINT OIL (UNII: AV092KU4JH)
  • LEMON OIL (UNII: I9GRO824LL)

Administration Route(s)

Additional informationCallout TooltipWhat 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

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Rebel Green Llc
Labeler Code: 72772
FDA Application Number: part333A Additional informationCallout TooltipWhat 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. Additional informationCallout TooltipWhat 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: 01-21-2019 Additional informationCallout TooltipWhat 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: 12-31-2020 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Rebel Green Hand Sanitizer Peppermint And Lemon Product Label Images

Rebel Green Hand Sanitizer Peppermint And Lemon 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

ALCOHOL (70%)

Purpose

HAND SANITIZER

Uses

TO SANITIZE HANDS

Directions

WHEN YOU CAN'T USE SIMPLE SOAP AND WATER, HAND SANITIZER IS AN EXCELLENT ALTERNATIVE.

Warnings

IN CASE OF EYE CONTACT, FLUSH WELL WITH WATER.IN CASE OF INGESTION, DRINK A GLASS OR WATER AND IF NECESSARY, CONTACT YOUR PHYSICIAN.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN AND PETS.

Questions?

GIVE US A CALL AT 844-240-9992 OR VISIT OUR WEBSITE AT REBELGREEN.COM

Inactive Ingredients

PURIFIED WATER, GLYCERIN, ISOPROPYL ALCOHOL, CARBOMER, 2-AMINO-2-METHYL-PROPANOL, ORGANIC PEPPERMINT AND LEMON ESSENTIAL OIL

* Please review the disclaimer below.

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