OTC Medication Information: BZK Towelette

BZK TOWELETTE — benzalkonium chloride solution
H and P Industries, Inc. dba Triad Group

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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
  • apply over large areas of the body
  • use longer than 1 week unless directed by a doctor.

Ask a doctor in case of

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor

if condition persists or gets worse

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
  • if bandaged, let dry first

INACTIVE INGREDIENTS

purified water, sodium bicarbonate

CARTON INFORMATION

TRIAD

Cat. No. 10-5201

NDC 50730-5201-0

Antiseptic

BENZALKONIUM

CHLORIDE TOWELETTE

Helps prevent the risk of skin infection

For Professional and Hospital Use Only

Triad Disposables, Inc.

Brookfield, WI 53045 USA

Contents:

100 towelettes

carton
(click image for full-size original)
BZK TOWELETTE benzalkonium chloride solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:50730-5201
Route of Administration TOPICAL, EPIDURAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
benzalkonium chloride (benzalkonium) benzalkonium chloride .0013 mL
Inactive Ingredients
Ingredient Name Strength
sodium bicarbonate
water
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:50730-5201-0 100 POUCH (POUCH) in 1 CARTON contains a POUCH
1 1 SOLUTION (SWAB) in 1 POUCH This package is contained within the CARTON (50730-5201-0)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 08/28/1997
Labeler — H and P Industries, Inc. dba Triad Group (050259597)
Registrant — H and P Industries, Inc. dba Triad Group (050259597)
Establishment
Name Address ID/FEI Operations
H and P Industries, Inc. dba Triad Group 050259597 manufacture

Revised: 12/2009 H and P Industries, Inc. dba Triad Group

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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