FDA.reportPublic FDA data

4165 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 21:13:38

Label at a glance#

Product4165 First Aid Kit
Active ingredientWATER, ALCOHOL
Label structure18 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

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

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

Paws Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 66.5%

Paws Purpose

OTC - PURPOSE SECTION

Antiseptic

Paws Uses

INDICATIONS & USAGE SECTION

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

Paws 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

Paws 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

Paws Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe vera, fragrance, purified water, triethanolamine

Paws Questions

OTC - QUESTIONS SECTION

1-800-430-5490

4074 SF00001122 Kit Contents

SPL UNCLASSIFIED SECTION

1 BUFFERED EYE WASH 1 OZ BTL

1 BANDAGE COMP, 2" OFFSET, 4 PER

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

1 WATER JEL DRESSING,2" X 6"

1 CPR KIT-MASK, GLOVES, WIPES

LBL STOCK 6-3/8"X4"

1 LBL STOCK 3"x1-7/8"

1 LABEL RAPID FAK 16U/25P

1 PR LRG NITRILE GLVES ZIP BAG

1 KIT STL 16 UN (HORIZONTAL)

Eyewash Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

EyesalineEyesaline

Paws Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PawsPaws

4165 Kit Label Z019805

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4165 label4165 label

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0498-41650498-4165-01
0498-01000498-0100-02
0498-3111

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM PHOSPHATE, DIBASICGR686LBA74IACT
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE593YOG76RNIACT
WATER059QF0KO0RACTIB
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

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
199ce24b-12fb-82b7-e063-6294a90a59a388b53bc0-2c7f-9a9b-e053-2a95a90a91a42024-05-29WarningsExact identifier
spl set id: 88b53bc0-2c7f-9a9b-e053-2a95a90a91a4

Reported adverse events (FAERS/openFDA)#

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