NDC 71857-0015 Diapia Adl Hand Cleanerspray

Ethyl Alcohol

NDC Product Code 71857-0015

NDC 71857-0015-1

Package Description: 100 mL in 1 BOTTLE

NDC Product Information

Diapia Adl Hand Cleanerspray with NDC 71857-0015 is a a human over the counter drug product labeled by Bsg H & B Co., Ltd.. The generic name of Diapia Adl Hand Cleanerspray is ethyl alcohol. The product's dosage form is spray and is administered via topical form.

Labeler Name: Bsg H & B Co., Ltd.

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.

Diapia Adl Hand Cleanerspray 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.

  • WATER (UNII: 059QF0KO0R)

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: Bsg H & B Co., Ltd.
Labeler Code: 71857
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: 10-30-2020 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.

Diapia Adl Hand Cleanerspray Product Label Images

Diapia Adl Hand Cleanerspray 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

Inactive Ingredient

Water, Glycerin, Sodium Hyaluronate, Centella Asiatica Extract, Saururus Chinensis Extract, Fragrance

Otc - Purpose

Antibacterial, Antiseptic, Kills 99.9% of germs

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Spray on the palm of the hand.Rub hands together covering all surfaces of the nads and fingers.Rub until your hands are dry.

Warnings

Keep out of reach of children.Store in a cool, dry place and avoid direct sunlight.Do not inhale or drink it.Discontinue use if skin allergy or discomfort occurs.

Dosage & Administration

For external use only

* Please review the disclaimer below.