NDC 76123-245 Bzk Antiseptic

NDC Product Code 76123-245

NDC CODE: 76123-245

Proprietary Name: Bzk Antiseptic 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

  • 76123 - School Health Corporation

NDC 76123-245-01

Package Description: 10 BOX in 1 CASE > 100 PACKET in 1 BOX > .75 mL in 1 PACKET

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

NDC Product Information

Bzk Antiseptic with NDC 76123-245 is a product labeled by School Health Corporation. 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: 1038558.

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)

Product Labeler Information

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

Labeler Name: School Health Corporation
Labeler Code: 76123
Start Marketing Date: 04-05-2011 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: 12-31-2018 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.

Bzk Antiseptic Product Label Images

Bzk Antiseptic 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

Otc - Active Ingredient

Active Ingredient                                     PurposeBenzalkonium Chloride 0.13% v/v              Antiseptic

Use: Towelette

  • First aid antiseptic to help prevent skin infection in minor cuts, scrapes and burnsAntiseptic cleansingPerineal and maternity care

Warnings

For external use only

Indications And Usage

  • General antisepticAsk a doctor before use if you havedeep or puncture woundsanimal bitesserious burns

Stop Use If

  • Stop Use if:irritation and redness developif condition persists for more than 72 hours, consult a physician.

Directions

  • Directions:Tear at notch, remove towelette, use only onceAs a first aid antisepticclean affeected areaapply 1 to 3 times dailymay be covered with a sterile bandageif bandaged let dry first

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.

Do Not Use

  • Do not useas a first aid antiseptic for more than 1 weekin the eyesover large areas of the body

Inactive Ingredient Section

Inactive ingredient(s):water

* Please review the disclaimer below.