Label: 4148 FIRST AID KIT- 4148 first aid

  • NDC Code(s): 0498-0100-01, 0498-0121-00, 0498-0501-00, 0498-0733-00, view more
    0498-4148-01
  • Packager: Honeywell Safety Products USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated May 4, 2019

If you are a consumer or patient please visit this version.

  • Sting Relief Active ingredient (in each wipe)

    Ethyl alcohol 50.0%

    Lidocaine HCl 2.0%

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  • Sting Relief Purposse

    Antiseptic

    Topical pain relief

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  • Sting Relief Uses

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

    For external use only


    Flammable, keep away from open fire or flame

    Do not use

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

    Stop use and ask a doctor

    • 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.

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

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  • Sting Relief Directions

    • 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.

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  • Sting Relief Inactive ingredients

    benzalkonium chloride, menthol, and purified water

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  • Sting Relief Questions or Comments?

    1-800-430-5490

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  • Eyewash Active ingredient

    Sterile Water 99%

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  • Eyewassh Purpose

    Eyewash

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  • Eyewash Uses

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

    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

    • 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

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

    Keep out of reach of children

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

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  • Eyeash Directions

    • 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
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  • Eyewash Inactive ingredients

    sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

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  • Eyeash Questions

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

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  • PVP Active ingredient

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

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  • PVP Purpose

    First aid antiseptic

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  • PVP Uses

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


    For external use only.

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if

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

    Keep out of reach of children.

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

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  • PVP Directions

    • 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
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  • PVP Other 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

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  • PVP Inactive ingredients

    nonoxynol 9, water

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  • BZK Active ingredient

    Benzalkonium chloride 0.13% w/v

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  • BZK Purpose

    First aid antiseptic

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  • BZK Uses


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

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  • BZK Warnings

    For external use only

    Do not use

    • 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

    • if irritation, redness or other symptoms develop
    • the condition persists or gets worse

    Keep out of reach of children

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

    • tear open packet and use as a washcloth
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  • BZK Other information

    • store at room temperature 15 0 to 30 0 C (59 0 - 86 0 F)
    • do not reuse towelette
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  • BZK Inactive ingredient

    water

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  • 4148 SF00003879 Kit Contents

    5 TRIANGULAR BDG, NON-STERILE

    1 ADH TAPE, .5" X 2.5 YD, 2 PER

    1 GAUZE COMPRESS, 1728 SQ IN 1

    1 FORCEPS & SCISSORS, 1 EA

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

    1 GAUZE COMP, 18" X 36", 2 PER

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

    1 PVP IODINE WIPES 10 PER

    1 STING RELIEF WIPES 10 PER BOX

    1 NITRILE GLOVES 2PR BBP

    2 ANTIMCRBL ANTSPTC TWLETTS

    1 MICROSHIELD BAGGED 72-151

    5 IVYX CLEAN TOWEL 300/CS

    1 1 OZ, BUFF EYEWASH

    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

    1 SHIELD/SURGICAL MASK

    2 COLD PACK UNIT 4"X6" BULK

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  • Sting Relief Principal Display Panel
  • Eyewash Principal Display Panel
  • PVP Principal Display Panel
  • BZK Principal Display Panel
  • 4148 Kit Label SF00003879
  • INGREDIENTS AND APPEARANCE
    4148 FIRST AID KIT 
    4148 first aid kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4148
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-4148-01 1 in 1 KIT 09/13/2018
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 1 BOTTLE 30 mL
    Part 2 10 POUCH 4 mL
    Part 3 10 POUCH 3 mL
    Part 4 2 PACKET 2.8 mL
    Part 1 of 4
    EYESALINE EMERGENCY EYEWASH 
    purified water liquid
    Product Information
    Item Code (Source) NDC:0498-0100
    Route of Administration OPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 98.6 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0100-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part349 12/18/2018
    Part 2 of 4
    STING RELIEF PAD 
    ethyl alcohol, lidocaine swab
    Product Information
    Item Code (Source) NDC:0498-0733
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  in 1 mL
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    MENTHOL (UNII: L7T10EIP3A)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0733-00 0.4 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part348 12/23/2017
    Part 3 of 4
    PVP IODINE WIPE 
    povidone-iodine 10% swab
    Product Information
    Item Code (Source) NDC:0498-0121
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 10 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    NONOXYNOL-9 (UNII: 48Q180SH9T)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0121-00 0.3 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 09/18/2018
    Part 4 of 4
    ANTISEPTIC TOWELETTE 
    benzalkonium chloride liquid
    Product Information
    Item Code (Source) NDC:0498-0501
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0501-00 1.4 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 12/22/2017
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 09/13/2018
    Labeler - Honeywell Safety Products USA, Inc. (079287321)
    Registrant - Honeywell Safety Products USA, Inc. (079287321)
    Establishment
    Name Address ID/FEI Business Operations
    Honeywell Safety Products USA, Inc 079287321 pack(0498-4148)
    Establishment
    Name Address ID/FEI Business Operations
    Honeywell Safety Products USA, Inc. 167518617 manufacture(0498-0100)
    Establishment
    Name Address ID/FEI Business Operations
    Changzhou Maokang Medical 421317073 manufacture(0498-0501)
    Establishment
    Name Address ID/FEI Business Operations
    Sion Medical Biotext 532775194 manufacture(0498-0121)
    Establishment
    Name Address ID/FEI Business Operations
    Safetec of America Inc 874965262 manufacture(0498-0733)
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