NDC 62428-711 Glacier Blue Antibacterial Foaming Hand Wash

Benzalkonium Chloride

NDC Product Code 62428-711

NDC Code: 62428-711

Proprietary Name: Glacier Blue Antibacterial Foaming Hand Wash Additional informationCallout TooltipWhat 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.

Non-Proprietary Name: Benzalkonium Chloride Additional informationCallout TooltipWhat is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.


Code Structure
  • 62428 - Lawson Product, Inc
    • 62428-711 - Glacier Blue Antibacterial Foaming Hand Wash

NDC 62428-711-03

Package Description: 750 mL in 1 BOTTLE, PUMP

NDC 62428-711-29

Package Description: 1000 mL in 1 BAG

NDC 62428-711-57

Package Description: 550 mL in 1 BOTTLE, PUMP

NDC Product Information

Glacier Blue Antibacterial Foaming Hand Wash with NDC 62428-711 is a a human over the counter drug product labeled by Lawson Product, Inc. The generic name of Glacier Blue Antibacterial Foaming Hand Wash is benzalkonium chloride. The product's dosage form is soap and is administered via topical form.

Labeler Name: Lawson Product, Inc

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 Additional informationCallout TooltipWhat 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.


Glacier Blue Antibacterial Foaming Hand Wash Active Ingredient(s)

Additional informationCallout TooltipWhat 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 .13 1/mL

Inactive Ingredient(s)

Additional informationCallout TooltipAbout 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)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • COCAMINE OXIDE (UNII: QWA2IZI6FI)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
  • PEG-4 RAPESEEDAMIDE (UNII: 89575CN928)
  • COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • CITRIC ACID ACETATE (UNII: DSO12WL7AU)
  • ALCOHOL (UNII: 3K9958V90M)
  • IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
  • BENZYL ACETATE (UNII: 0ECG3V79ZJ)
  • SODIUM GLYCOLATE (UNII: B75E535IMI)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • TRISODIUM NITRILOTRIACETATE (UNII: E3C8R2M0XD)
  • DIETHYL PHTHALATE (UNII: UF064M00AF)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Administration Route(s)

Additional informationCallout TooltipWhat 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

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Lawson Product, Inc
Labeler Code: 62428
FDA Application Number: part333E Additional informationCallout TooltipWhat 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. Additional informationCallout TooltipWhat 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: 04-01-2019 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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.

Glacier Blue Antibacterial Foaming Hand Wash Product Label Images

Glacier Blue Antibacterial Foaming Hand 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

Glacier Blue Antibacterial Foaming Hand Wash Active Ingredient

Benzalkonium Chloride 0.13%

Glacier Blue Antibacterial Foaming Hand Wash Purpose

Antibacterial

PurposeAntibacterial

Glacier Blue Antibacterial Foaming Hand Wash Warnings

  • For external use only. Do not ingest.Avoid contact with eyes. If contact occurs, rinse thoroughly with water.Stop use and ask a doctor if irritation and redness develop.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 Poison Control Center right away.

Glacier Blue Antibacterial Foaming Hand Wash 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.

Glacier Blue Antibacterial Foaming Hand Wash Inactive Ingredients

Water, Phenoxyethanol, Cocamine Oxide, Propylene Glycol, Decyl Glucoside, PEG-4 Rapeseedamide, Cocamidopropyl Hydroxysultaine, Glycerin, Fragrance, Sodium Chloride, Tetrasodium EDTA, Citric Acid, Ethanol, Iodopropynyl Butylcarbamate, Benzyl Acetate, Sodium Glycolate, Sodium Hydroxide, Trisodium Nitrilotriacetate, Diethyl Phthalate, FD&C Blue #1.

Glacier Blue Antibacterial Foaming Hand Wash Questions

Questions? 888-GO BETCO (888-462-3826)

Glacier Blue Antibacterial Foaming Hand Wash Keep Out Of Reach Of Childen

KEEP OUT OF REACH OF CHILDREN

Glacier Blue Antibacterial Foaming Hand Wash Package Label

75929_Drummond_GlacierBlueAntibacterial

* Please review the disclaimer below.

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