NDC 73167-100 Bob Barker Antibacterial Wrapped Body


NDC Product Code 73167-100

NDC 73167-100-01

Package Description: 1000 CELLO PACK in 1 CASE > 1 APPLICATOR in 1 CELLO PACK > 11 g in 1 APPLICATOR

NDC 73167-100-02

Package Description: 500 CELLO PACK in 1 CASE > 1 APPLICATOR in 1 CELLO PACK > 29 g in 1 APPLICATOR

NDC 73167-100-03

Package Description: 144 CELLO PACK in 1 CASE > 1 APPLICATOR in 1 CELLO PACK > 75 g in 1 APPLICATOR

NDC 73167-100-04

Package Description: 144 CELLO PACK in 1 CASE > 1 APPLICATOR in 1 CELLO PACK > 85 g in 1 APPLICATOR

NDC Product Information

Bob Barker Antibacterial Wrapped Body with NDC 73167-100 is a a human over the counter drug product labeled by Pt Megasurya Mas. The generic name of Bob Barker Antibacterial Wrapped Body is chloroxylenol. The product's dosage form is soap and is administered via cutaneous form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 2172091.

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.

Bob Barker 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.

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 OIL (UNII: 5QUO05548Z)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Cutaneous - Administration to the skin.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Pt Megasurya Mas
Labeler Code: 73167
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: 06-01-2017 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 08-01-2022 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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".

* Please review the disclaimer below.

Bob Barker Antibacterial Wrapped Body Product Label Images

Bob Barker 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


Drug Facts

Active Ingredient

Chloroxylenol 0.1%




For washing to decrease bacteria on skin.


For External Use Only.

Otc - Do Not Use

Do not use this product on infants under 6.

Otc - When Using

When using this product avoid contact with eyes. In case of eye contact, flush with water.

Otc - Stop Use

Stop use and ask doctor if irritation and redness develops.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.


  • Wet bar with waterLather vigorously and wash skinRinse and dry thoroughly

Inactive Ingredients

Sodium Palmate, Calcium Carbonate, Water, Sodium Palm Kernelate, Palm (Elaeis Guineesis) Oil, Sodium Lauryl Sulfate, Glycerin, Sodium Chloride, Titanium Dioxide, Fragrance, Tetrasodium EDTA, Etidronic Acid

* Please review the disclaimer below.