FDA.reportPublic FDA data

4268 First Aid Kit

Manufacturer
Honeywell Safety Products USA, Inc.
Effective date
2024-01-22
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:13:26

Label at a glance#

Product4268 First Aid Kit
Active ingredientALCOHOL, BENZALKONIUM CHLORIDE
Label structure19 sections

Indications and uses

for handwashing to decrease bacteria on skin whenever soap and water is not readily available

Dosage and administration

wet hands and wrists thoroughly for 15 seconds and allow to air dry always reseal after use children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 66.5%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on skin whenever soap and water is not readily available

Warnings

WARNINGS SECTION

For external use only


Flammable: keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

  • in the eyes. If this happens, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness develop and persists for more than 72 hours

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


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

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands and wrists thoroughly for 15 seconds and allow to air dry
  • always reseal after use
  • children under 6 years of age should be supervised when using this product

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe vera, fragrance, purified water, triethanolamine

Questions

OTC - QUESTIONS SECTION

1-800-430-5490

BZK Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13% w/v

BZK Purpose

OTC - PURPOSE SECTION

First aid antiseptic

BZK Uses

INDICATIONS & USAGE SECTION

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

BZK Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • 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

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • if irritation, redness or other symptoms develop
  • the condition persists or gets worse

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

BZK Directions

DOSAGE & ADMINISTRATION SECTION

  • tear open packet and use as a washcloth

BZK Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature 15 0 to 30 0 C (59 0 - 86 0 F)
  • do not reuse towelette

BZK Inactive ingredient

INACTIVE INGREDIENT SECTION

water

BZK Questions

OTC - QUESTIONS SECTION

1-800-430-5490

4268 SF00000669 Kit Contents

SPL UNCLASSIFIED SECTION

3 PAWS PERS ANTIMICRO WIPE

LBL STOCK 6-3/8"X4"

LBL STOCK 3"x1-7/8"

1 BZK ANTISEPTIC WIPE, BULK

2 PR LRG NITRILE GLVES ZIP BAG

1 FACEMASK W/SHLD EAR LOOP

1 PICK-UP SCOOP W/SCRAPER

1 SOLIDIFIER BBP POUCH 2 OZ ID E

1 KIT, PP 10 UNIT FA

2 BAG BIOHAZARD 24 X 24 RED

2 TOWEL 3-FOLD WHITE

2 TWIST TIE

PAWS Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PAWSPAWS

BZK Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antiseptic WipeAntiseptic Wipe

4268 Kit Label SF00000669

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4268 label4268 label

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0498-42680498-4268-01
61010-3111
0498-05010498-0501-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOEV5VD430YW9IACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML · Source PDF

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1a02c9d9-9b8d-0eaa-e063-6294a90a6393866997d0-397c-0684-e053-2a91aa0a69132024-06-03WarningsExact identifier
spl set id: 866997d0-397c-0684-e053-2a91aa0a6913
AntimicrobialALCOHOLSafetec of America, Inc.4a070d45-f7fd-4eab-a2ba-48445d54fe5d2024-02-05WarningsExact identifier
ndc (product): 61010-3111

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.