4396 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 21:13:44

Label at a glance#

Product4396 First Aid Kit
Active ingredientPOVIDONE-IODINE, LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE
Label structure27 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

PVP Wipes Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Povidone-iodine 10%

(equivalent to 1% titratable iodine)

PVP Wipes Purpose

OTC - PURPOSE SECTION

First aid antiseptic

PVP Wipes Uses

INDICATIONS & USAGE SECTION

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

PVP Wipes 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 Wipes 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 Wipes Other information

OTHER SAFETY INFORMATION

  • 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 Wipes Inactive ingredients

INACTIVE INGREDIENT SECTION

nonoxynol 9, water

PVP Wipes Questions

OTC - QUESTIONS SECTION

800-430-5490

Burn Cream Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Lidocaine hydrochloride 0.5%

Burn Cream Purpose

OTC - PURPOSE SECTION

First aid antiseptic

External analgesic

Burn Cream Uses

INDICATIONS & USAGE SECTION

  • prevent skin infection
  • for temporary relief of pain associated with miinor burns

Burn Cream Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • in or near the eyes
  • if you are allergic to any of the ingredients
  • in large areas of the body particularly over raw surfaces or blistered areas
  • for more than 10 days

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 persists
  • symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of chidren

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Burn Cream Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years of age and older:
  • clean the affected area
  • apply a small amount of this product (equal to the area of the tip of finger) onto the affected area 1 to 3 times daily
  • may be covered with a sterile bandage
  • children under 2 years of age: ask a doctor

Burn Cream Other information

OTHER SAFETY INFORMATION

  • tamper evident sealed packets
  • do not use if packet is opened or torn

Burn Cream Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis juice, cetyl alcohol, diazolidinyl urea, edetate disodium, glycerin, glyceryl stearate SE, methylparaben, mineral oil, PEG-100, propylene glycol, propylparaben, stearic acid, trolamine, water

Burn Cream Questions

OTC - QUESTIONS SECTION

1-800-430-5490

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 Otheer information

SPL UNCLASSIFIED SECTION

  • store at room temperature away from light

Ammonia Innactive 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

4396 011798-1494 Kit Contents

SPL UNCLASSIFIED SECTION

1 43 LBL KIT BOX 011798-1494

1 44 LBL BOEING WARNING

1 237 LBL INNER 011798-1494

1 201 LBL OUTER 011798-1494

1 FIRST AID BURN CREAM 6 PER

1 AMMONIA INHALANTS 10 PER

4 GAUZE BANDAGE, 4" X 6 YD

5 TRIANGULAR BDG, NON-STERILE

2 WIRE SPLINT 1 PER

1 ADHESIVE TPE 1"X2-1/2 YD 2 PER

8 BANDAGE COMP, 4" OFFSET, 1 PER

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

2 PVP IODINE WIPES 10 PER

1 SCISSOR BDGE 4" RED PLS HDL

LBL STOCK 6-3/8"X4"

1 LBL STOCK 6-3/8"X4"

1 LBL STOCK 3"x1-7/8"

1 STOCK LABEL 1 7/8" X 1/2"

1 PR LRG NITRILE GLVES ZIP BAG

1 KIT STL 24 UN WHITE 01

1 LABL INSTR 24 & 36 UNIT KITS

Honeywell PVP Wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Honeywell PVP wipeHoneywell PVP wipe

Burn Cream Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Burn CreamBurn Cream

Ammonia Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ammonia InhalentAmmonia Inhalent

4396 Kit Label 011798-1494

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4396 label4396 label

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0498-43960498-4396-01
0498-01210498-0121-00, 0498-0121-34
0498-0903

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 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
1a13d379-1534-3081-e063-6294a90a272f93402333-ba17-ede8-e053-2995a90aa8d22024-06-04WarningsExact identifier
spl set id: 93402333-ba17-ede8-e053-2995a90aa8d2

Reported adverse events (FAERS/openFDA)#

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