NDC 72288-196 Hand Sanitizer
Alcohol Gel Topical

Product Information

What is NDC 72288-196?

The NDC code 72288-196 is assigned by the FDA to the product Hand Sanitizer which is a human over the counter drug product labeled by Amazon Services Llc. The generic name of Hand Sanitizer is alcohol. The product's dosage form is gel and is administered via topical form. The product is distributed in a single package with assigned NDC code 72288-196-01 6 carton in 1 box / 160 pouch in 1 carton / 1.2 ml in 1 pouch. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code72288-196
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.
Hand Sanitizer
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.
Alcohol
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
Dosage FormGel - 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) 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.
Amazon Services Llc
Labeler Code72288
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.
part333A
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.
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.
06-14-2021
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.
12-31-2024
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".
N
NDC Code Structure

What are the uses for Hand Sanitizer?


Product Packages

NDC Code 72288-196-01

Package Description: 6 CARTON in 1 BOX / 160 POUCH in 1 CARTON / 1.2 mL in 1 POUCH

Product Details

What are Hand Sanitizer Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Hand Sanitizer Active Ingredients UNII Codes

Hand Sanitizer Inactive Ingredients UNII Codes

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.

* Please review the disclaimer below.

Hand Sanitizer Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Active Ingredient



Ethyl Alcohol 70%


Purpose



Antiseptic


Use



hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.


Warnings



For external use only.

Flammable. Keep away from fire or flame.


Do Not Use



  • in children less than 2 months of age
  • on open skin wounds

Otc - When Using



When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.


Otc - Stop Use



Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.


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.


Directions



  • Apply entire contents of pouch onto hands and rub briskly until dry.
  • Children under 6 years of age should be supervised when using this product.

Other Information:



  • Store below 110°F (43°C)
  • May discolor certain fabrics and surfaces

Inactive Ingredients



Alicyle Acrylate, Aminomethyl, Caprylyl Glycol, Crosspolymer, Fragrance, Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Propanol, Tocopherol Acetate, Water(Aqua)


Otc - Questions



Questions?: 800-719-9260

NDC #72288-196-01


Principal Display Panel - 1.2 Ml Pouch Label



TEAR
HERE

Amazon
basic care

Kills 99.99%

of Germs

Compare to

Purell* Singles

active Ingredient

Advanced

Hand

Sanitizer
Gel With
Moisturizers

Contains 70% Ethanol

Not tested on Animals

Made in USA

1.2 mL (.04 fl oz.)


* Please review the disclaimer below.