4219 First Aid Kit

Manufacturer
Honeywell Safety Products USA, INC
Effective date
2024-01-22
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 21:13:21

Label at a glance#

Product4219 First Aid Kit
Active ingredientWATER, BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, ALCOHOL, LIDOCAINE HYDROCHLORIDE, HYDROCORTISONE ACETATE
Label structure36 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Eyewash Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sterile Water 99%

Eyewash Purpose

OTC - PURPOSE SECTION

Eyewash

EyewashUses

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

1-800-430-5490

Triple Active ingredient (each gram contains)

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

OTC - ASK DOCTOR SECTION

  • 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

Questions or Comments?

OTC - QUESTIONS SECTION

1-800-430-5490

Hydrocortisone Cream Active ingredient (in each gram)

OTC - ACTIVE INGREDIENT SECTION


Hydrocortisone acetate (equivalent to Hydrocortisone 1%)

Hydrocortisone 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

Hysrocortisone 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 ..

Hydrocortisone Questions or Comments?

OTC - QUESTIONS SECTION

1-800-430-5490

4219 013061-4454 Kit Contents

SPL UNCLASSIFIED SECTION

1 FNGRTIP-5 PER, KNCKL BDG-4 PER

1 TRIPLE ANTIBIOTIC 10 PER

1 TRIANGULAR BDG, NON-STERILE

1 BANDAGE COMP, 3" OFFSET, 2 PER

1 ADHESIVE BDG,PLSTIC,1"X3"16PER

1 ADH BAND, EXTRA LARGE, 6 PER

1 1 OZ EYE WASH W/PADS & STRIPS

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

1 NITRILE GLOVES 2PR BBP

1 CPR MICROSHIELD W/2 PR LTX GLV

1 BBP PROTECT APPAREL KIT

LBL STOCK 6-3/8"X4"

1 LBL STOCK 3"x1-7/8"

1 LABEL RAPID BLANK 24U/50P

1 KIT STL 24 UN WHITE 01

1 STING RELIEF 10

Eyewash Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Eyewash LabelEyewash Label

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

Hydrocortisone Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HydrocortisoneHydrocortisone

4219 Kit Label 013061-4454

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4219 label4219 label

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Ingredients#

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Source Document#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1a0268d3-0854-8564-e063-6294a90a770b84ae7b5d-4199-fe09-e053-2a91aa0add652024-06-03WarningsExact identifier
spl set id: 84ae7b5d-4199-fe09-e053-2a91aa0add65

Reported adverse events (FAERS/openFDA)#

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