NDC 75709-002 Instant Hand Sanitizer

Instant Hand Sanitizer

NDC Product Code 75709-002

NDC 75709-002-01

Package Description: 60 mL in 1 BOTTLE

NDC 75709-002-02

Package Description: 70 mL in 1 BOTTLE

NDC 75709-002-03

Package Description: 100 mL in 1 BOTTLE

NDC 75709-002-04

Package Description: 150 mL in 1 BOTTLE

NDC 75709-002-05

Package Description: 300 mL in 1 BOTTLE

NDC 75709-002-06

Package Description: 520 mL in 1 BOTTLE

NDC Product Information

Instant Hand Sanitizer with NDC 75709-002 is a a human over the counter drug product labeled by Xi'an Explution Tech Co.,ltd.. The generic name of Instant Hand Sanitizer is instant hand sanitizer. The product's dosage form is gel and is administered via topical form.

Labeler Name: Xi'an Explution Tech Co.,ltd.

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.

Instant 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: Xi'an Explution Tech Co.,ltd.
Labeler Code: 75709
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: 04-30-2020 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.

Instant Hand Sanitizer Product Label Images

Instant 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

Alcohol 80%v/v.




Hand Sanitizer to help reduce bacteria on skin.


For external use only.Flammable.Keep away from heat or flame.

When Using This Product

Do not use on open skin Wounds.Keep out of eyes.ln.case of contact with eyes.rinse eyes thoroughly with water.Use with caution if allergic to alcohoL.

Otc - Stop Use

Stop use and ask a doctor if irritation of rash appears and tasts.

Keep Out Of Reach For Children

If swallowed.get medical help or contact a Poison Control Center right away.


1.Pump enough amount of product in your palm to thoroughly spread on both hands.2.Rub thoroughly over all surfaces of both hands.3.Rub hands together briskly until dry.

Other Information

Store below 106°F.(41°C)May discolor certain fabrics or surface.

Inactive Ingredients

Glycerin.hydrogen peroxide, purified water.

* Please review the disclaimer below.