NDC 92763-008 Disinfectant

Disinfectant

NDC Product Code 92763-008

NDC 92763-008-01

Package Description: 355 mL in 1 BOTTLE

NDC Product Information

Disinfectant with NDC 92763-008 is a a human over the counter drug product labeled by Nanofixit Ventures Inc.. The generic name of Disinfectant is disinfectant. The product's dosage form is spray and is administered via topical form.

Labeler Name: Nanofixit Ventures Inc.

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Disinfectant 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 141.5 g/355mL

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.

  • BUTANE (UNII: 6LV4FOR43R)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)
  • WATER (UNII: 059QF0KO0R)
  • PROPANE (UNII: T75W9911L6)
  • ISOBUTANE (UNII: BXR49TP611)

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: Nanofixit Ventures Inc.
Labeler Code: 92763
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: 09-04-2020 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.

Disinfectant Product Label Images

Disinfectant 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

Dosage & Administration

Do not store above the following temperature: 50°C [122°F) Store in accordance with local regulations.Use appropriate containment to avoid environmental contamination.Store away from direct sunlight in a dry, cool and well-ventilated area, away from food and drink. Eliminate all ignition sources.

Inactive Ingredient

WaterButanePropaneIsobutaneSodium benzoateTriethanolamineParfum(LEMON)

Indications & Usage

Shake well. Hold can upright 6" to 8”from surface. Spray 2 to 3 seconds until covered with mist.To deodorize: spray on surface as needed.To sanitize: let stand for 30 seconds then allow to air dry.

Otc - Active Ingredient

Ethanol

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Otc - Purpose

Disinfection

Sterilization

No Rinseing

Warnings

FLAMMABLE AEROSOL CONTAINS PRESSURED GAS MAY EXPLODE IF HEATED

* Please review the disclaimer below.