NDC 72265-103 Quash Multi Sanitizer

Ethanol

NDC Product Code 72265-103

NDC 72265-103-01

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Quash Multi Sanitizer with NDC 72265-103 is a a human over the counter drug product labeled by Curescript. The generic name of Quash Multi Sanitizer is ethanol. The product's dosage form is spray and is administered via topical form.

Labeler Name: Curescript

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.

Quash Multi 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 20.4 g/30mL

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ALLANTOIN (UNII: 344S277G0Z)
  • ALOE (UNII: V5VD430YW9)
  • TEA TREE OIL (UNII: VIF565UC2G)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)

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: Curescript
Labeler Code: 72265
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: 02-01-2021 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".

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Quash Multi Sanitizer Product Label Images

Quash Multi 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

Ethanol 68% (w/w)

Inactive Ingredients

Water, Glycerin,Allantoin,Water,Fragrance,Aloe Extract, TEA TREE OIL,Sodium Hyaluronate,Centella asiatica Extract,Eucalyptus Oil

Purpose

Antiseptic

Warnings

For external use only-handsFlammable. Keep away from heat and flame.When using this product ■ Keep out of eyes. In case of contact with eyes, flush thoroughly with water. ■ Avoid contact with broken skin. ■ Do not inhale or ingest.Stop use and ask a doctor if skin irritation or rash develops.Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Keep Out Of Reach Of Children

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

Uses

■ Hand sanitizer to decrease bacteria on the skin that could cause disease

Directions

■ Spray enough product in your hands to thoroughly cover your hands.■ rub hands together briskly until dry■ Supervise children under 6 years of age when using this product to avoid swallowing.■ no recommended for infants

Other Information

■ Store between 15-30C (59-86F)■ Avoid freezing and excessive heat above 40C (104F)■ May discolor certain fabrics or surfaces

Questions

Www.getquash.comtel) +820218117395

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