Bzk Plus Prep Pad
FDA Label NDC 50730-5151

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by H And P Industries, Inc. Dba Triad Group for the product Bzk Plus Prep Pad (NDC 50730-5151). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, do not use, consult a doctor in case of, otc - ask doctor/pharmacist, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Benzalkonium chloride .13% w/v

Purpose

Antiseptic

Use

First Aid Antiseptic to help prevent the risk of infection in minor cuts, scrapes and burns

Warnings

For external use only.


Do Not Use

  • in the eyes
  • longer than 1 week unless directed by a doctor

Consult A Doctor In Case Of

  • deep or puncture wounds
  • animal bites
  • serious burns

Otc - Ask Doctor/Pharmacist


Otc - When Using


Stop Use And Ask A Doctor

If condition persists or gets worse

Otc - Pregnancy Or Breast Feeding


Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • clean the affected area
  • apply a small amount of this product to the area 1-3 times daily
  • may be covered with a sterile bandage when dry

Other


Inactive Ingredients

Nonoxynol-9, purified water, sodium bicarbonate

Otc - Questions


Pouch Information

TRIAD PLUSCat. No. 11-PZ32NDC 50730-5151-8BENZALKONIUM CHLORIDEPREP PADAntiseptic0.13% Benzalkonium Chloride, w/v1 PadTriad Disposables, Inc.Brookfield, WI 53045Made in USAwww.triad-group.net

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