NDC 72265-104 Quash Multi Sanitizing Tissue

Alcohol

NDC Product Code 72265-104

NDC 72265-104-01

Package Description: 20 CLOTH in 1 PACKET

NDC Product Information

Quash Multi Sanitizing Tissue with NDC 72265-104 is a a human over the counter drug product labeled by Curescript. The generic name of Quash Multi Sanitizing Tissue is alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Curescript

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.

Quash Multi Sanitizing Tissue 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 .54 1/1

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)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • MENTHOL (UNII: L7T10EIP3A)
  • 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
  • POLOXAMER 184 (UNII: BIS92ZSF57)
  • PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • THYME (UNII: CW657OBU4N)
  • SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)

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 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’.

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Quash Multi Sanitizing Tissue Product Label Images

Quash Multi Sanitizing Tissue 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 54.7% (v/v)

Inactive Ingredients

Water,Glycerin,Sodium Benzoate,PEG-60 Hydrogenated Castor Oil ,Fragrance,Citric acid,Menthol,1,2-Hexanediol,Poloxamer 184,PEG-7 Glyceryl Cocoate,Aloe Barbadensis Leaf Extract,Thymus Vulgaris (Thyme) Extract,Sophora Flavescens Root Extract,Sodium Hyaluronate,Cocamidopropyl Betaine,Butylene Glycol,Sodium Chloride

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

■ Help decrease bacteria on the hands

Directions

■ Rive the seal■ Pull out the wet tissue towel through small opening■ Rub thoroughly over all surfaces of both hands with the we wipes.■ Supervise children under 6 years of age when using this product to avoid swallowing.

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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