NDC 72797-001 Bobbarker Antibacterial Wrapped Body

Benzethonium Chloride

NDC Product Code 72797-001

NDC Code: 72797-001

Proprietary Name: Bobbarker Antibacterial Wrapped Body 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: Benzethonium Chloride 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.


Code Structure
  • 72797 - Yangzhou H&r Plastic Dailychemicall Co., Ltd.
    • 72797-001 - Bobbarker Antibacterial Wrapped Body

NDC 72797-001-01

Package Description: 1000 PACKAGE in 1 BOX > 11.06 g in 1 PACKAGE

NDC 72797-001-02

Package Description: 500 PACKAGE in 1 BOX > 29.78 g in 1 PACKAGE

NDC 72797-001-03

Package Description: 144 PACKAGE in 1 BOX > 81.04 g in 1 PACKAGE

NDC 72797-001-04

Package Description: 144 PACKAGE in 1 BOX > 85.07 g in 1 PACKAGE

NDC 72797-001-05

Package Description: 200 PACKAGE in 1 BOX > 81.05 g in 1 PACKAGE

NDC 72797-001-06

Package Description: 500 PACKAGE in 1 BOX > 35.44 g in 1 PACKAGE

NDC Product Information

Bobbarker Antibacterial Wrapped Body with NDC 72797-001 is a a human over the counter drug product labeled by Yangzhou H&r Plastic Dailychemicall Co., Ltd.. The generic name of Bobbarker Antibacterial Wrapped Body is benzethonium chloride. The product's dosage form is soap and is administered via topical form.

Labeler Name: Yangzhou H&r Plastic Dailychemicall Co., Ltd.

Dosage Form: Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.

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.


Bobbarker Antibacterial Wrapped Body 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.

  • BENZETHONIUM CHLORIDE .1 g/100g

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)
  • PALM ACID (UNII: B6G0Y5Z616)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • COCONUT ACID (UNII: 40U37V505D)
  • SODIUM PALMATE (UNII: S0A6004K3Z)
  • SODIUM COCOATE (UNII: R1TQH25F4I)
  • SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)

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: Yangzhou H&r Plastic Dailychemicall Co., Ltd.
Labeler Code: 72797
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: 03-05-2019 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.

Bobbarker Antibacterial Wrapped Body Product Label Images

Bobbarker Antibacterial Wrapped Body 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

Benzethonium Chloride 0.1%

Purpose

Antibacterial

Uses

For washing to decrease bacteria on the skin.

Warnings

For external use only.

When Using This Product

Avoid contact with eyes. In case of eye contact, flush with water.Don't use this product on infants under 6 months of age.

Stop Use And Ask A Doctor

If irritation and redness develops.

Keep Out Of Reach Of Children.

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

Directions

  • Wet bar with waterlather vigorously and wash skinrinse and dry thoroughly.

Inactive Ingredients

Soap (Sodium Palmate and/or Sodium Tallowate, Sodium Cocoate and/or Sodium Palm Kernelate), Water, Palm Acid, Glycerin, Sodium Chloride, Coconut Acid, Fragrance, Tetrasodium EDTA, Citric Acid Anhydrous

* Please review the disclaimer below.

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