NDC 0869-0492 Foaming Hand Sanitizer

NDC Product Code 0869-0492

NDC CODE: 0869-0492

Proprietary Name: Foaming 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

  • 0869 - Vi-jon

NDC 0869-0492-21

Package Description: 90 mL in 1 PACKAGE

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

NDC Product Information

Foaming Hand Sanitizer with NDC 0869-0492 is a product labeled by Vi-jon. 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: 1020365.

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)
  • DMDM HYDANTOIN (UNII: BYR0546TOW)
  • CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
  • ISOCETETH-20 (UNII: O020065R7Z)
  • DISODIUM COCOAMPHODIPROPIONATE (UNII: 6K8PRP397M)
  • PPG-2 HYDROXYETHYL COCO/ISOSTEARAMIDE (UNII: EK4J71ZKEQ)
  • LAURETH-23 (UNII: N72LMW566G)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)

Product Labeler Information

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

Labeler Name: Vi-jon
Labeler Code: 0869
Start Marketing Date: 09-03-2014 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: 12-31-2019 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.

Foaming Hand Sanitizer Product Label Images

Foaming 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

Claims

For questions, please visit www.mycleanpath.com or call (213) 568-0006.  Manufactured by Vi-Jon, Inc. St. Louis MO 63114To Dilute: Flip bottle, squeeze pod to fill measuring cup.  Remove pump, add distilled water to fill line.  Air bubble in cup is normal.  CleanPath Refill pod only to be used with CleanPath Reusable Bottle.  Do not use for any other purpose.effctive at eliminating 99.9% of many common harmful germs in as little as 15 seconds

Active Ingredient

Concentrate: Benzalkonium chloride 1.3%Use Dilution: Benzalkonium chloride 0.13%

Purpose

Antiseptic

Use

For handwashing to decrease bacteria on the skin

Warnings

For external use only

When Using This Product

  • Do not use in the eyes.  In case of contact with eyes, flush thoroughly with wateravoid contact with broken skindilute with distilled water before use because acidic or hard water may render the product inactive

Stop Use And Ask A Doctor If

Condition persists for more than 72 hours

Keep Out Of Reach Of Children

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

Directions

  • Follow dilution instructionswet hands thoroughly with product and allow to dry without wiping

Inactive Ingredients

Water, DMDM hydantoin, fragrance, cetrimonium chloride, isoceteth-20, disodium cocamphodipropionate, PPG-2 hydroxyethyl coco/isostearamide, laureth-23, citric acid, blue 1, ext. violet 2, red 40

Adverse Reaction

Manufactured by Vi-Jon, Inc.St. Louis, MO 63114

* Please review the disclaimer below.