NDC 18949-710 Maintenance Warehouse

Benzalkonium Chloride

NDC Product Code 18949-710

NDC 18949-710-04

Package Description: 3780 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Maintenance Warehouse with NDC 18949-710 is a a human over the counter drug product labeled by Hd Supply Facilities Maintenance, Ltd. The generic name of Maintenance Warehouse is benzalkonium chloride. The product's dosage form is soap and is administered via topical form.

Labeler Name: Hd Supply Facilities Maintenance, Ltd

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.


Maintenance Warehouse 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.

  • BENZALKONIUM CHLORIDE 1.3 mg/mL

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 LAURYL SULFATE (UNII: 368GB5141J)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PEG-4 RAPESEEDAMIDE (UNII: 89575CN928)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • COCONUT ACID (UNII: 40U37V505D)
  • ALCOHOL (UNII: 3K9958V90M)
  • BRONOPOL (UNII: 6PU1E16C9W)
  • DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)
  • MAGNESIUM NITRATE (UNII: 77CBG3UN78)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)

Administration Route(s)

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

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Hd Supply Facilities Maintenance, Ltd
Labeler Code: 18949
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: 04-15-2019 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: N 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.

Maintenance Warehouse Product Label Images

Maintenance Warehouse 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

Antibacterial Hand Soap Active Ingredient

​Active Ingredient​Benzalkonium Chloride 0.13%

Antibacterial Hand Soap

  • Uses​​Antibacterial hand cleaner.
  • Use in daycare, hospitals, nursing homes, physicians offices, dental offices and clinics

  • WarningsFor external use only.Avoid contact with eyes.Children under the age of 6 should be supervised by an adult when using this product.Discontinue use is irritation or redness develops.If irritation persists for more than 72 hours, consult a physician.KEEP OUT OF REACH OF CHILDREN.
  • If swallowed, get medical help or contact a Posion Control Center right away.

  • Directions​Read the entire label before using this product.​Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands.Rinse with clean water.

Inactive Ingredients​Water, Sodium Lauryl Sulfate, Cocamidopropyl Betaine, Propylene Glycol, Sodium Chloride, Glycerin, PEG-4 Rapeseedamide, Dimethicone PEG-7 Cocoate, Ethanol, Fragrance, Bronopol, Diisoporpanolamine, Magnesium Nitrate, FD&C Yellow #5, Methychloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone, FD&C Red #40.

888-GO-BETCO (888-462-3826)Betco.com

PurposeAntibacterial

KEEP OUT OF REACH OF CHILDREN

74404_HD Supply Maintenance_Warehouse

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