FDA.reportPublic FDA data

4164 First Aid Kit

Manufacturer
Honeywell Safety Products USA, Inc. | Honeywell Safety Products US, Inc.
Effective date
2021-12-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:23:20

Label at a glance#

Product4164 First Aid Kit
Active ingredientAMMONIA, BENZALKONIUM CHLORIDE
Label structure20 sections

Indications and uses

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

Dosage and administration

tear open packet and use as a washcloth

Label contents#

Full prescribing information#

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

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 i

OTC - DO NOT USE SECTION

f 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.

Ammoniia 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 UNCLASSIFIED 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

4164 SF00004064 Kit contents

SPL UNCLASSIFIED SECTION

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

1 NITRILE GLOVES 2PR BBP

2 ANTIMCRBL ANTSPTC TWLETTS

1 SCISSOR BDGE 4" RED PLS HDL

LBL STOCK 6-3/8"X4"

1 LBL STOCK 3"x1-7/8"

3 PAD LOCK PLASTIC SEAL

2 WATER-JEL BURN DRESSING 4 X 4

1 WATER-JEL BURN DRESSING 2 X 6

4 LABEL "FIRST AID" EACH SIDE

1 EXPIRATION STICKER NP31TH

1 LABEL ON INSIDE LID CTY1872-5

1 SERVICE RECORD PLACARD ATY1160

1 KIT PP 24 UNIT FA

BZK Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antiseptic WipeAntiseptic Wipe

Ammonia Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ammonia InhalantAmmonia Inhalant

4164 Kit Label SF00004064

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4164 label4164 label

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0498-41640498-4164-01
0498-33340498-3334-00
0498-05010498-0501-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
AMMONIA5138Q19F1XACTIB
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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0ea124f0-4998-0e75-e063-6394a90ad46d88055371-ca11-6d17-e053-2a95a90ad23a2024-01-10WarningsExact identifier
spl set id: 88055371-ca11-6d17-e053-2a95a90ad23a

Reported adverse events (FAERS/openFDA)#

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