NDC 73700-002 Benemax Advanced Hand Sanitizer

Isopropyl Alcohol

NDC Product Code 73700-002

NDC 73700-002-01

Package Description: 1000 mL in 1 BOTTLE, SPRAY

NDC Product Information

Benemax Advanced Hand Sanitizer with NDC 73700-002 is a a human over the counter drug product labeled by Nugale Pharmaceutical Inc. The generic name of Benemax Advanced Hand Sanitizer is isopropyl alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Nugale Pharmaceutical Inc

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.

Benemax Advanced 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.


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.

  • ALOE (UNII: V5VD430YW9)
  • 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: Nugale Pharmaceutical Inc
Labeler Code: 73700
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: 07-15-2020 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.

Benemax Advanced Hand Sanitizer Product Label Images

Benemax Advanced 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

Isopropyl alcohol 70%, USP




As a hand sanitizer when there is no water, to reduce bacteria on the skin which can cause illness. Recommended for repeated use.


Flammable, keep away from fire or flameFor external use only

When Using This Product

  • Do not use in or near the eyes, or inhalein case of contact, rinse eyes thoroughly with water

Stop Use And Ask A Doctor

If a rash on irritation appear and remain at the site of contact

Keep Out Of Reach Of Children.

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


  • Dispense sufficient liquid to cover the hands, rub hands together briskly for 30 seconds.     Allow hands to dry. • children under 6 years of age must be upervised when using this product.

Other Information

  • Do not store above 1100F (430C). May discolor certain fabrics or substances

Inactive Ingredient

Aloe (aloe barbadensis) Juice, D-alpha-tocopheryl Acetate, Glycerin, PEG, Water

* Please review the disclaimer below.