4175 FIRST AID KIT- 4175 first aid kit 
Honeywell Safety Products USA, Inc

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

----------

0498-4175: First Aid Kit (BZKwipes- 019735-0022L)

Active ingredient

Benzalkonium chloride 0.13% w/v

Purpose

First aid antiseptic

Uses

Antiseptic cleansing of face, hands and body without soap and water

Do not use

  • in the eyes or over large areas of the body
  • on mucous membranes
  • on irritated skin
  • in case of deep puncture wounds, animal bites or serious burns, consult a doctor
  • longer than 1 week unless directed by a doctor

Warnings

For external use only

Stop use and ask a doctor if

  • irritation, redness or other symptoms develop
  • the 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

Other information

Inactive ingredient

water

Questions

1-800-430-5490

4175
019735-0022L kit contents

1 ANTIMCRBL ANTSPTC TWLETTS 6PER

1 NITRILE GLOVES 2PR BBP

2 CPR MICROSHIELD W/2 PR LTX GLV

LBL STOCK 4"X2-7/8"

1 LBL STOCK 3"x1-7/8"

1 KIT STL UN 6 WHITE

1 INSTR LABEL FA REV B

1 LABEL 6U CVR NORTH CPR DLX

Package Labeling

BZK label

4175 Kit Label
019735-0022L

4175 label

4175 FIRST AID KIT 
4175 first aid kit kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-4175
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0498-4175-011 in 1 KIT12/22/2017
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 16 PACKET 8.4 mL
Part 1 of 1
ANTISEPTIC TOWELETTE 
benzalkonium chloride liquid
Product Information
Item Code (Source)NDC:0498-0501
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0498-0501-001.4 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/22/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/22/2017
Labeler - Honeywell Safety Products USA, Inc (118768815)

Revised: 1/2024
Document Id: 0f8eb488-30f1-b3db-e063-6294a90a0117
Set id: 87874df0-6e42-2a42-e053-2a95a90a84b2
Version: 6
Effective Time: 20240122
 
Honeywell Safety Products USA, Inc