NDC 68604-237 Hand Kleen Foaming Instant Hand Sanitizer

NDC Product Code 68604-237

NDC CODE: 68604-237

Proprietary Name: Hand Kleen Foaming Instant Hand Sanitizer 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.

NDC Code Structure

  • 68604 - Auto-chlor System, Llc
    • 68604-237 - Hand Kleen Foaming Instant Hand Sanitizer

NDC 68604-237-01

Package Description: 1000 mL in 1 BAG

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

NDC Product Information

Hand Kleen Foaming Instant Hand Sanitizer with NDC 68604-237 is a product labeled by Auto-chlor System, Llc. 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: 1041869.

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)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
  • MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG)
  • LANOLIN (UNII: 7EV65EAW6H)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)

Product Labeler Information

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

Labeler Name: Auto-chlor System, Llc
Labeler Code: 68604
Start Marketing Date: 12-31-2012 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.

Hand Kleen Foaming Instant Hand Sanitizer Product Label Images

Hand Kleen Foaming Instant Hand Sanitizer 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

Benzethonium Chloride 0.20% w/w

Otc - Purpose

Antiseptic handwash

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.

Indications & Usage

For handwashing to decrease bacteria on the skin.

Warnings

For external use only.When using this product:Do not get into eyes.If contact occurs, rinse thoroughly with water.

Dosage & Administration

Apply small amount to palm.Briskly rub, covering hands with product until dry.

Inactive Ingredient

Water, Propylene Glycol, Phenoxyethanol, Cocamidopropyl Betaine, Sodium Chloride, Glycerin, PEG-7 Glyceryl Cocoate, Meadowfoamamidopropyl Betaine, Lanolin, Dimethicone, Disodium Laureth Sulfosuccinate, Fragrance, Dye

* Please review the disclaimer below.