NDC 11084-115 Panache Antibacterial Body Wash

NDC Product Code 11084-115

NDC 11084-115-05

Package Description: 3780 mL in 1 BOTTLE, PLASTIC

NDC 11084-115-07

Package Description: 2000 mL in 1 CARTRIDGE

NDC 11084-115-27

Package Description: 1000 mL in 1 CARTRIDGE

NDC 11084-115-34

Package Description: 118 mL in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Panache Antibacterial Body Wash with NDC 11084-115 is a product labeled by Deb Usa, Inc.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1050670.

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)
  • SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • COCO DIETHANOLAMIDE (UNII: 92005F972D)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Product Labeler Information

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

Labeler Name: Deb Usa, Inc.
Labeler Code: 11084
Start Marketing Date: 01-01-2010 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: 12-31-2017 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Panache Antibacterial Body Wash Product Label Images

Panache Antibacterial Body Wash 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

Otc - Active Ingredient

Active ingredientTriclosan 0.5%

Otc - Purpose

Antibacterial

Indications & Usage

UsesFor washing to decrease bacteria on the skin

Warnings

WarningsFor external use onlyAvoid contact with the eyes

Otc - Keep Out Of Reach Of Children

Keep out of reach of childrenConsult with a physician if ingested

Dosage & Administration

DirectionsDispense product onto washcloth or directly onto skinLather and wash for 15-20 secondsRinse thoroughly

Inactive Ingredient

Water, Sodium Laureth Sulfate, Propylene Glycol, Disodium Laureth Sulfosuccinate, Sodium Chloride, Cocamide DEA, Cocamidopropyl Betaine, Fragrance, Tetrasodium EDTA, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, FDC Red No. 40, FDC Yellow No. 5.

* Please review the disclaimer below.