NDC 61139-513 Highmark Professional Premium Foam Antibacterial Handwash

  1. Labeler Index
  2. Office Max, Inc.
  3. NDC: 61139-513 Highmark Professional Premium Foam Antibacterial Handwash

NDC Product Code 61139-513

NDC CODE: 61139-513

Proprietary Name: Highmark Professional Premium Foam Antibacterial Handwash 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.
Non-Proprietary Name: What 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.

NDC Code Structure

NDC 61139-513-10

Package Description: 1000 mL in 1 BOTTLE

NDC 61139-513-20

Package Description: 2000 mL in 1 BOTTLE

NDC 61139-513-80

Package Description: 800 mL in 1 BAG

NDC 61139-513-89

Package Description: 1200 mL in 1 BOTTLE

NDC 61139-513-90

Package Description: 1250 mL in 1 BOTTLE

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

NDC Product Information

Highmark Professional Premium Foam Antibacterial Handwash with NDC 61139-513 is a product labeled by Office Max, Inc.. The generic name of Highmark Professional Premium Foam Antibacterial Handwash is . The product's dosage form is and is administered via form.

Labeler Name: Office Max, Inc.

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.
  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • AMMONIUM LAURETH-2 SULFATE (UNII: 698O4Z48G6)
  • AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM)
  • COCO MONOETHANOLAMIDE (UNII: C80684146D)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • LACTIC ACID (UNII: 33X04XA5AT)
  • VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
  • JOJOBA OIL (UNII: 724GKU717M)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
  • CORN OIL (UNII: 8470G57WFM)
  • AMMONIUM SULFATE (UNII: SU46BAM238)
  • METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
  • METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
  • FD&C RED NO. 4 (UNII: X3W0AM1JLX)
  • FD&C YELLOW NO. 6 (UNII: H77VEI93A8)

Product Labeler Information

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

Labeler Name: Office Max, Inc.
Labeler Code: 61139
Start Marketing Date: 11-22-2013 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 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.

Highmark Professional Premium Foam Antibacterial Handwash Product Label Images

Highmark Professional Premium Foam Antibacterial Handwash 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

Active Ingredient

Chloroxylenol 0.3%

Purpose

Antimicrobial

Use

Handwash to help decrease bacteria on the skin.Recommended for repeated use.

Directions

Wet handsApply product and thoroughly cover hands with latherRinse well and dry hands completely

Inactive Ingredients

Water (Aqua), Alcohol, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Propylene Glycol, Algae Extract, Aloe Barbadensis Leaf Juice, Ammonium Xylenesulfonate, Cocamide MEA, Glycerin, Isopropyl Alcohol, Lactic-Acid, Retinyl Palmitate, Simmondsia Chinensis (Jojoba) Seed Oil, Tetrasodium EDTA, Tocopheryl Acetate, Zea Mays (Corn) Oil, Ammonium Sulfate, Fragrance (Parfum) Methylchloroisothiazolinone, Methylisothiazolinone, Red 4 (CI 14700), Yellow 6 (CI 15985)

Package Label

For general hand washing and germ killing

Warnings

For external use only

Otc - When Using

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or rash appears and lasts

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.

* Please review the disclaimer below.