NDC 10819-6007 Sani Professional Hands Instant Sanitizing Wipes

Alcohol

NDC Product Code 10819-6007

NDC CODE: 10819-6007

Proprietary Name: Sani Professional Hands Instant Sanitizing Wipes 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.

Non-Proprietary Name: Alcohol 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.

NDC Code Structure

  • 10819 - Professional Disposables International, Inc.
    • 10819-6007 - Sani Professional Hands Instant Sanitizing Wipes

NDC 10819-6007-1

Package Description: 484 mL in 1 CANISTER

NDC Product Information

Sani Professional Hands Instant Sanitizing Wipes with NDC 10819-6007 is a a human over the counter drug product labeled by Professional Disposables International, Inc.. The generic name of Sani Professional Hands Instant Sanitizing Wipes is alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Professional Disposables International, Inc.

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

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.

Sani Professional Hands Instant Sanitizing Wipes 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 .7 mL/mL

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.

  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • WATER (UNII: 059QF0KO0R)
  • ALOE ARBORESCENS LEAF (UNII: 09TD8L5SQV)
  • ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • ALOE ARBORESCENS LEAF (UNII: 09TD8L5SQV)
  • WATER (UNII: 059QF0KO0R)
  • ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • GLYCERIN (UNII: PDC6A3C0OX)

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: Professional Disposables International, Inc.
Labeler Code: 10819
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: 03-01-2020 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: 12-31-2020 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.

Sani Professional Hands Instant Sanitizing Wipes Product Label Images

Sani Professional Hands Instant Sanitizing Wipes 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

Alcohol 70% by volume

Purpose

Antiseptic

Uses

Hand sanitizer to decrease bacteria on the skinfor repeated usedries in seconds

Warnings

Flammable, keep away from fire or flameFor external use onlydo not use in or contact the eyesdiscontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

Keep Out Of Reach Of Children

Keep this out of reach of childrenIf swallowed, get medical help or contact a poison control center right away

Directions

Canister:to dispense, lift cover, remove seal, pull center sheet from roll, twist to a point, feed through dispenser hole in cover. Keep cap closed to prevent moisture loss.use entire wipe to thoroughly wipe hands, fingers, and wriststo sanitize, use multiple wipesdiscard after single usePacket:open packetuse entire wipe to thoroughly wipe hands, fingers, and wriststo sanitize, use multiple wipesdiscard after single use

Other Information

Lot No. and Expiration Date can be found on canister

Inactive Ingredients

Aloe barbadensis leaf juice, glycerin, propylene glycol, tocopheryl acetate, water

* Please review the disclaimer below.