NDC 65133-130 Aire-master Sanitizer Gel Vit E/a


NDC Product Code 65133-130

NDC 65133-130-01

Package Description: 3784 mL in 1 BOTTLE, PLASTIC

NDC 65133-130-02

Package Description: 120 mL in 1 BOTTLE, PLASTIC

NDC 65133-130-03

Package Description: 208120 mL in 1 DRUM

NDC 65133-130-04

Package Description: 251 mL in 1 BOTTLE, PUMP

NDC 65133-130-05

Package Description: 251 mL in 1 BOTTLE, PUMP

NDC 65133-130-06

Package Description: 1000 mL in 1 POUCH

NDC 65133-130-07

Package Description: 60 mL in 1 BOTTLE, PLASTIC

NDC 65133-130-08

Package Description: 1892 mL in 1 BOTTLE, PLASTIC

NDC 65133-130-09

Package Description: 81 mL in 1 BOTTLE, PLASTIC

NDC 65133-130-10

Package Description: 946000 mL in 1 TANK

NDC 65133-130-11

Package Description: 500 mL in 1 BOTTLE, PUMP

NDC 65133-130-12

Package Description: 473 mL in 1 BOTTLE, PUMP

NDC 65133-130-13

Package Description: 37 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Aire-master Sanitizer Gel Vit E/a with NDC 65133-130 is a a human over the counter drug product labeled by Aire-master Of America, Inc. The generic name of Aire-master Sanitizer Gel Vit E/a is alcohol. The product's dosage form is gel and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 581658.

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.

Aire-master Sanitizer Gel Vit E/a 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.

  • 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.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Aire-master Of America, Inc
Labeler Code: 65133
FDA Application Number: part333E 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: 01-01-1998 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 - NO 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".

* Please review the disclaimer below.

Aire-master Sanitizer Gel Vit E/a Product Label Images

Aire-master Sanitizer Gel Vit E/a 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

Ethanol 60%



Indications & Usage

Handwash to help reduce bacteria that potentially can cause disease.


Flammable, keep away from fire or flame.For external use only.Do not use in eyes.  In case of eye contact flush thoroughly with water and seek medical attention.Stop use and ask doctor if irritation and redness develop and persists for more than 72 hours.

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.


  • Dispense an adequate amount in your palm to cover all surfaces of hands completely.Rub hands together until dry.Does not require rinsing.

Other Information

  • Do not Store above 105 F.May discolor some fabrics.

Inactive Ingredients

Water, Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Fragrance, Tocopheryl Acetate, Retinyl Palmitate.


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* Please review the disclaimer below.