4362 First Aid Kit

Manufacturer
Honeywell Safety Products USA, Inc.
Effective date
2021-12-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:21:13

Label at a glance#

Product4362 First Aid Kit
Active ingredientBENZALKONIUM CHLORIDE, WATER, POLYMYXIN B SULFATE, BACITRACIN ZINC, NEOMYCIN SULFATE, ISOPROPYL ALCOHOL, LIDOCAINE HYDROCHLORIDE, ALCOHOL, HYDROCORTISONE ACETATE, AMMONIA, POVIDONE-IODINE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
Label structure80 sections

Indications and uses

temporarily relieves pain due to minor burns

Dosage and administration

adults and children 2 years of age and older; apply to affected area not more than 3 to 4 times daily children under 2 years of age: ask a doctor you may report a serious reaction to this product to 800-430-5490

Label contents#

Full prescribing information#

Burn Jel Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 2.0%

Burn Jel Purpose

OTC - PURPOSE SECTION

External analgesic

Burn Jel Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves pain due to minor burns

Burn Jel Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on large areas of the body, particularly over raw surfaces or blistered areas

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • the condition gets worse
  • symptoms persist for more than 7 days
  • condition clears up and recurs within a few days

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.

Burn JEl Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years of age and older; apply to affected area not more than 3 to 4 times daily
  • children under 2 years of age: ask a doctor
  • you may report a serious reaction to this product to 800-430-5490

Burn Jel Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature - do not use if opened or torn

Burn Jel Inactive ingredients

INACTIVE INGREDIENT SECTION

carbopol 940, carbopol 1342, diazolidinyl urea, glycerin, melaleuca alternifolia (tea tree) leaf oil, methylparaben, octoxynol-9, propylene glycol, propylparaben, trolamine, water

Burn Jel Questions

OTC - QUESTIONS SECTION

1-800-430-5490

Triple Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Bacitracin zinc 400 units

Neomycin sulfate (5 mg equivalent to 3.5 mg Neomycin base)

Polymyxin B sulfate 5000 units

Triple Purpose

OTC - PURPOSE SECTION

First aid antibiotic

First aid antibiotic

First aid antibiotic

Triple Uses

INDICATIONS & USAGE SECTION


first aid to help prevent infection in:

  • minor cuts
  • scrapes
  • burns

Triple Warnings

WARNINGS SECTION

For external use only

Allergy alert: do not use if you are allergic to any of the ingredients

Do not use

OTC - DO NOT USE SECTION

  • in the eyes
  • over large areas of the body
  • Ask a doctor before use if you have
  • a deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • the condition persists or gets worse
  • a rash or other allergic reaction develops
  • you need to use longer than 1 week

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Triple Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area
  • apply a small amount of the product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily
  • may be covered with a sterile bandage

Triple Other information

SPL UNCLASSIFIED SECTION

  • store at 15 0 to 25 0 C (59 0 to 77 0 F)
  • tamper evident sealed packets
  • do not use if packet is torn or opened

Triple Inactive ingredient

INACTIVE INGREDIENT SECTION

petrolatum

Triple Questions?

OTC - QUESTIONS SECTION

1-800-430-5490

Sting Relief Active ingredient (in each wipe)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 50.0%

Lidocaine HCl 2.0%

Sting Relief Purpose

OTC - PURPOSE SECTION

Antiseptic

Topical pain relief

Sting Relief Uses

INDICATIONS & USAGE SECTION

  • prevent infection in minor scrapes, and temporary relief of itching of insect bites

Sting Relief Warnings

WARNINGS SECTION

For external use only


Flammable, keep away from open fire or flame

Do not use

OTC - DO NOT USE SECTION

  • over large areas of the body
  • in eyes
  • over raw or blistered areas

Stop use and ask a doctor

OTC - STOP USE SECTION

  • if conditions worsen or persist for more than 7 days or clear up and occur again within a few days

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.

Sting Relief Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years and older: Apply to cleaned affected area not more than 3 times daily.
  • children under 2 years of age: consult a doctor.

Sting Relief Inactive ingredients

INACTIVE INGREDIENT SECTION

benzalkonium chloride, menthol, and purified water

Sting Relief Questions or Comments?

OTC - QUESTIONS SECTION

1-800-430-5490

Eyewash Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sterile Water 99%

Eyewash Purpose

OTC - PURPOSE SECTION

Eyewash

Eyewash Uses

INDICATIONS & USAGE SECTION

  • for flushing the eye to remove loose foreign material, air pollutants or chlorinated water

Eyewash Warnings

WARNINGS SECTION

For external use only

  • Obtain immediate medical treatment for all open wounds in or near eyes.
  • To avoid contamination, do not touch tip of container to any surface.
  • Do not reuse.
  • Once opened, discard.

Do not use

OTC - DO NOT USE SECTION

  • if solution changes color or becomes cloudy
  • if you have open wounds in or near the eyes, get medical help right away.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you experience eye pain
  • changes in vision
  • continued redness or irritation of the eye
  • condition worsens or persists

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.

Eyewash Directions

DOSAGE & ADMINISTRATION SECTION

  • remove contacts before using
  • twist top to remove
  • flush the affected area as needed
  • control rate of flow by pressure on the bottle
  • if necessary, continue flushing with emergency eyewash or shower

Eyewash Inactive ingredients

INACTIVE INGREDIENT SECTION

sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

Eyewash Questions

OTC - QUESTIONS SECTION

Call 1-800-430-5490 Honeywell Safety Products USA, Inc. Smithfield, RI 02917

Hydrocortisone Active ingredient (in each gram)

OTC - ACTIVE INGREDIENT SECTION

Hydrocortisone acetate (equivalent to Hydrocortisone 1%)

Hydrcortisone Purpose

OTC - PURPOSE SECTION

Anti-itch cream

Hydrocortisone Uses

INDICATIONS & USAGE SECTION

  • for the temporary relief of itching associated with minor skin irritations and rashes

Hydrocortisone Warnings

WARNINGS SECTION


For external use only

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

  • you are using any other hydrocortisone product

When using the product

OTC - WHEN USING SECTION

  • avoid contact with eyes
  • do not begin use of any other hydrocortisone product unless you have consulted a doctor
  • do not use for the treatment of diaper rash

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • condition persists for more than 7 days
  • condition clears up and recurs within a few days

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.

Hydrocortisone Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years and older:
  • clean the affected area
  • apply to the area not more than 3 to 4 times daily
  • children under 2 years of age: consult a doctor

Hydrocortisone Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature (do not freeze)

Hydrocortisone Inactive ingredients

INACTIVE INGREDIENT SECTION

cetyl alcohol, citric acid, diazolidinyl urea, edetate disodium, glycerin, glyceryl monostearate, methylparaben, mineral oil, polyethylene glycol, propylene glycol, propylparaben, purified water, stearic acid, trolamine

Hydrocortisone Questions or Comments?

OTC - QUESTIONS SECTION

1-800-430-5490

Ammonia Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ammonia 15%

Ammonia Purpose

OTC - PURPOSE SECTION

Respiratory stimulant

Ammonia Uses

INDICATIONS & USAGE SECTION

  • to prevent or treat fainting

Ammonia Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • if you have breathing problems such as asthma or emphysema

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition persists

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.

Ammonia Directions

DOSAGE & ADMINISTRATION SECTION

hold inhalant away from face and crush ampoule between thumb and forefinger at position indicated on sleeve.

hold near nostrils for inhalation of volatile vapor

Ammonia Other information

SPL PATIENT PACKAGE INSERT SECTION

  • store at room temperature away from light

Ammonia Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol USP, FD&C red #40, lavender oil, lemon oil fcc, nutmeg oil, purified water

Ammonia Questions or Comments?

OTC - QUESTIONS SECTION

1-800-430-5490

Alcohol Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70%

Alcohol Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Alcohol Uses

INDICATIONS & USAGE SECTION

first aid to help prevent infection in

  • minor cuts
  • scrapes
  • burns

Alcohol Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire and flame

Do not use

OTC - DO NOT USE SECTION

  • in or near eyes
  • over large areas of the body

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

OTC - WHEN USING SECTION

  • do not use longer than 1 week unless directed by a doctor

Stop use and consult a doctor if

OTC - STOP USE SECTION

  • 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

Alcohol Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area
  • may be covered with a sterile bandage
  • apply wipe to affeted are 1 to 3 times daily
  • discard wipe after single use

Alcohol Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature 15 0 to 25 0 C (59 0 to 77 0 F)
  • do not use if packet is torn or opened

Alcohol Inactive ingredient

INACTIVE INGREDIENT SECTION

water

Alcohol Questions

OTC - QUESTIONS SECTION

1-800-430-5490

PVP Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Povidone-iodine 10% (equivalent to 1% titratable iodine)

PVP Purpose

OTC - PURPOSE SECTION

First aid antiseptic

PVP Uses

INDICATIONS & USAGE SECTION

  • first aid antiseptic to help prevent infection in minor cuts, scrapes and burns

PVP Warnings

WARNINGS SECTION


For external use only.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens or persists for more than 72 hours
  • irritation and redness develops

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.

PVP Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area
  • apply1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first
  • discard wipe after single use

PVP Other information

SPL UNCLASSIFIED SECTION

  • do not use on individuals who are allergic or sensitive to iodine
  • store at controlled temperature 59-86ºF (15-30ºC)
  • do not use if pouch is open or torn

PVP Inactive ingredients

INACTIVE INGREDIENT SECTION

nonoxynol 9, water

Sun X Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 1.0%

Homosalate 5.0%

Octinoxate 7.5%

Octisalate 5.0%

Oxybenzone 6.0%

Sun X Purpose

OTC - PURPOSE SECTION

Sunscreen

Sunscreen

Sunscreen

Sunscreen

Sunscreen

Sun X Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • If used as directed with other sun protection measures (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun.

Sun X Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

  • keep out of the eyes
  • rinse with water to remove

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rash occurs

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Sun X Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally and evenly 15 minutes before sun exposure

Sun Protection Measures: spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and after sun protection measures including:

  • limit time in the sun, especially from 10:00 a.m. - 2 p.m.
  • wear long-sleeved shirts, pants, hats and sunglasses.
  • reapply:
    • after 80 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours
  • children under 6 months of age: Ask a doctor

Sun X Other information

SPL UNCLASSIFIED SECTION

  • protect this product from excessive heat or direct sun

Sun x Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylates/C10-30 alkyl acrylate crosspolymer, aloe barbadensis leaf juice, butylparaben, calendula officinalis flower extract, carbomer, chamomile recutita extract, dimethicone, dimethyl capramide, ethylparaben, fragrance, glyceryl stearate, isobutylparaben, methylparaben, nasturtium officinale extract, peg-100 stearate, phenoxyethanol, propylparaben, symphytum officinale leaf extract, tetrasodium EDTA, triethanolamine, tocopherol, tocopherol acetate, water

Sun x Questions

OTC - QUESTIONS SECTION

1-877-684-5774

4293 SF00004080 Kit Contents

SPL UNCLASSIFIED SECTION

1 FNGRTIP-5 PER, KNCKL BDG-4 PER

1 TRIPLE ANTIBIOTIC 10 PER

1 AMMONIA INHALANTS 10 PER

1 EYE DRESS PKT W/4 ADH STRIPS

1 TRIANGULAR BDG, NON-STERILE

1 FORCEPS & SCISSORS, 1 EA

1 GAUZE BANDAGE, 2" X 6 YD,2 PER

1 INSTANT COLD PACK 4" X 6"

1 ADH BDG W/NOADHR PAD,1X3 32PER

1 BURN JEL 1/8 OZ, 6 PER

1 ALCOHOL PREP PADS 10P

1 HYDROCORTISON,1.O%,1/32 OZ,10P

1 PVP IODINE WIPES 10 PER

1 STING RELIEF WIPES 10 PER BOX

1 ADH TAPE W/P 1/2"X 2 1/2 YD

1 FIRST AID GUIDE ASHI

1 1 OZ, BUFF EYEWASH

1 BANDAGE COMP 4" W/TELFA PAD 1

LBL STOCK 6-3/8"X4"

LBL STOCK 4"X2-7/8"

1 LBL STOCK 3"x1-7/8"

1 KIT STL 24 UN WHITE 01

Burn Jel Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Burn JelBurn Jel

Triple Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Triple AntibioticTriple Antibiotic

Sting Relief Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sting ReliefSting Relief

Eyewash Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EyesalineEyesaline

Hydrocortisone Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hydrocortisone CreamHydrocortisone Cream

Ammonia Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ammonia InhalantAmmonia Inhalant

Alcohol Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol PrepsAlcohol Preps

PVP Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PVP WipePVP Wipe

Sun X Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sun XSun X

4293 Kit Label SF-00004080

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4293 label4293 label

Products#

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

DailyMed product names page 1 of 2 · 79 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 66 matching rows.

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0ec51fb8-48ec-3661-e063-6294a90a7a5b8a4916e4-95ce-fa26-e053-2995a90a1e7d2024-01-12WarningsExact identifier
spl set id: 8a4916e4-95ce-fa26-e053-2995a90a1e7d

Reported adverse events (FAERS/openFDA)#

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