NDC 81731-180 Bortek Hand Sanitizer

Ethanol

NDC Product Code 81731-180

NDC 81731-180-18

Package Description: 532 mL in 1 BOTTLE

NDC Product Information

Bortek Hand Sanitizer with NDC 81731-180 is a a human over the counter drug product labeled by Bortek Industries. The generic name of Bortek Hand Sanitizer is ethanol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Bortek Industries

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.

Bortek 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 70 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.

  • TROLAMINE (UNII: 9O3K93S3TK)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
  • WATER (UNII: 059QF0KO0R)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)

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: Bortek Industries
Labeler Code: 81731
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: 04-12-2021 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: 12-31-2022 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.

Bortek Hand Sanitizer Product Label Images

Bortek 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

Other

Drug Facts

Bortek Industries, Inc.800.626.7835sweeperland.com

Otc - Active Ingredient

Active IngredientEthyl Alcohol 70% v/v

Otc - Purpose

PurposeAntiseptic

Indications & Usage

  • UsesTo decrease bacteria on the skin that potentially can cause disease.Recommended for repeated use.

Warnings

  • WarningsFlammable, keep away from heat or flameFor external use only.

Otc - When Using

Keep out of eyes, ears or mouth. In case of contact, flush eyes with water.

Otc - Stop Use

Stop use and ask a doctor if irritation and redness develop or if condition persists for more than 72 hours.

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. Children should be supervised by an adult when using this product.

Dosage & Administration

  • DirectionsApply sufficient amount of product to your palm to cover both hands.Rub until dry.

Other Safety Information

Other informationMay discolor certain fabrics and surfaces.

Inactive Ingredient

Inactive ingredientsAcrylates/C10/30, Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, FD&C Blue No. 1, FD&C Yellow No. 5, Fragrance, Isopropyl Alcohol, PEG/PPG-18/18 Dimethicone, Triethanolamine, Vitamin E, Water

* Please review the disclaimer below.