NDC 37945-718 Antimicrobial Foaming Sanitizer

NDC Product Code 37945-718

NDC 37945-718-14

Package Description: 207 g in 1 BOTTLE

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

NDC Product Information

Antimicrobial Foaming Sanitizer with NDC 37945-718 is a product labeled by Bio-medical & Pharmaceutical Manufacturing Corporation. The generic name of Antimicrobial Foaming Sanitizer is . The product's dosage form is and is administered via form.

Labeler Name: Bio-medical & Pharmaceutical Manufacturing Corporation

Dosage Form: -

Product Type: 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.

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.

  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
  • 2-HEXENAL PROPYLENE GLYCOL ACETAL, (1E)- (UNII: ZBS49DF5S4)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • METHYLPARABEN (UNII: A2I8C7HI9T)

Product Labeler Information

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

Labeler Name: Bio-medical & Pharmaceutical Manufacturing Corporation
Labeler Code: 37945
Start Marketing Date: 10-09-2015 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: I 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.

Antimicrobial Foaming Sanitizer Product Label Images

Antimicrobial Foaming 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

Drug Facts

Foaming Antimicrobial Sanitizer

Active Ingredient

Benzethonium Chloride 0.2%

Otc - Purpose

Antimicrobial

Inactive Ingredients

Water,Lauramidopropyl Betaine, Propylene Glycol, Diazolidinyl Urea, Methylparaben,Propylparaben.

Purpose

First Aid Antimicrobial Sanitizer

Use

Kleer-Plex is a unique, non-drying sanitizer. Designed for all skin types and pH balanced. Kills 99.9% of germs including Staph,Pseudomonas, and E. coli. Excellent for post-operative care. May be used as a First Aid Antimicrobial to help protect againstskin infection.

Warnings

External use only. Do not use in eyes. In case of deep wounds or puncture wounds, consult a physician. If irritation develops and persists for more than a few days, discontinue use and consult a physician. .

Other Information

Alcohol FreeMoisturizesMade In USA

Otc - Questions

Questions or CommentsBio-Medical & Pharm., Mfg. Corp.4311 South Dr., Houston, TX 77053Phone: 281.835.8051Internet: www.kleerplex.com

Directions

Dispense foam into palms, then spread onto hands and other areas to be treated.

* Please review the disclaimer below.