NDC 80366-001 Clean Supply Hand Sanitizer


NDC Product Code 80366-001

NDC 80366-001-01

Package Description: 59 mL in 1 BOTTLE

NDC 80366-001-02

Package Description: 500 mL in 1 BOTTLE

NDC 80366-001-03

Package Description: 1892 mL in 1 CAN

NDC 80366-001-04

Package Description: 3786 mL in 1 CAN

NDC 80366-001-05

Package Description: 3 mL in 1 POUCH

NDC Product Information

Clean Supply Hand Sanitizer with NDC 80366-001 is a a human over the counter drug product labeled by Energy Alliance Technology Corp.. The generic name of Clean Supply Hand Sanitizer is alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Energy Alliance Technology Corp.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Clean Supply Hand Sanitizer 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.

  • ALCOHOL 80 mL/100mL

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.
  • 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: Energy Alliance Technology Corp.
Labeler Code: 80366
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: 09-01-2020 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: 12-31-2021 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Clean Supply Hand Sanitizer 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  80%




To help reduce bacteria and viruses on the skin that can potentially cause disease.


  • Do Not Use On children less than 2 months of age. On open wounds.Warning • For external use only. Flammable. Keep away from heat or flame.When using this productkeep out of eyes, ears, and mouth.In case of contact with eyes, rinse thoroughly with water.Stop use and ask a doctor if irritation or redness occurs.These may be signs of a serious condition.

Keep Out Of Reach Of Children.

  • If swallowed, get medical help or contact a poison control center immediately.


  • • For hands put enough product in the palm to coveryour hand and rub hands together briskly until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

  • • Store between 15 - 30 ̊C (59 - 86 ̊F).Avoid freezing and excessive heat above 40 ̊C (104 ̊F).May discolor certain fabrics or surfaces.

Inactive Ingredients

Deionized water, Isopropyl Alcohol, Glycol Alcohol, Acrylic Crosspolymer, Trolamine, Hydrogen Peroxide.

* Please review the disclaimer below.