Label: 4044 FIRST AID KIT- 4044 first aid kit
4045 FIRST AID KIT- 4045 first aid kit

  • NDC Code(s): 0498-0121-00, 0498-0121-34, 0498-0730-01, 0498-0903-34, view more
    0498-4044-01, 0498-4045-01
  • 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 November 28, 2018

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

  • PVP Wipes Active ingredient

    Povidone-iodine 10%

    (equivalent to 1% titratable iodine)

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  • PVP Wipes Purpose

    First aid antiseptic

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  • PVP Wipes Uses

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

    nonoxynol 9, water

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  • PVP Wipes Questions

    800-430-5490

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  • Burn Cream Active ingredient

    Benzalkonium chloride 0.13%

    Lidocaine hydrochloride 0.5%

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  • Burn Cream Purpose

    First aid antiseptic

    External analgesic

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  • Burn Cream Uses

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

    For external use only

    Do not use

    • 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

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if

    • 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

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

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  • Burn Cream Directions

    • 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
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  • Burn Cream Other information

    • tamper evident sealed packets
    • do not use if packet is opened or torn
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  • Burn Cream Inactive ingredients

    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

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  • Burn Cream Questions

    1-800-430-5490

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  • Neomycin Active ingredient

    Neonycin sulfate (5 mg equivalent to 3.5 mg Neomycin base)

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  • Neomycin Purpose

    First aid antibiotic

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  • Neomycin Uses

    first aid to help prevent infection in:

    • minor cuts
    • scrapes
    • burns
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  • Neomycin Warnings

    For external use only

    Neomycin
    Do not use

    • in the eyes
    • over large areas of the body

    Neomycin
    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    Neomycin
    Stop use and ask a doctor if:

    • the condition persists or gets worse
    • a rash or other allergic reaction develops
    • you need to use longer than 1 week

    Neomycin
    Keep out of reach of children

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

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  • Neomycin Directions

    • 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
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  • Neomycin Other information

    Store at 15 o to 25 o C (59 o to 77 oF)

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  • Neomycin Inactive ingredients

    petrolatum

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  • Neomycin Questions

    1-800-430-5490

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  • 4044 Z019733-0020L Kit Contents

    FIRST AID GUIDE ASHI

    GAUZE CLEAN-WRAP BDGE N/S 2"

    PVP PREP PADS MEDIUM 100/BX

    SCISSOR BDGE 4" RED PLS HDL

    FIRST AID CREAM 1.0GR PKT EACH

    TAPE ADHESIVE 1/2 X 2.5 125133

    POUCH NEOMYCIN ANTIBIOTIC .9 G

    ADH BNDG PLASTIC EX-LG 4"X 2"

    GAUZE PADS 3"X3" 12PLY

    PLASTIC BANDAGE 1" X 3"

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  • 4045 019733-0020L Kit Contents

    FIRST AID GUIDE ASHI

    GAUZE CLEAN-WRAP BDGE N/S 2"

    PVP PREP PADS MEDIUM 100/BX

    SCISSOR BDGE 4" RED PLS HDL

    FIRST AID CREAM 1.0GR PKT EACH

    TAPE ADHESIVE 1/2 X 2.5 125133

    POUCH NEOMYCIN ANTIBIOTIC .9 G

    ADH BNDG PLASTIC EX-LG 4"X 2"

    GAUZE PADS 3"X3" 12PLY

    PLASTIC BANDAGE 1" X 3"

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  • Honeywell PVP Wipes
  • Burn Cream Principal Display Panel
  • Neomycin Principal Display Panel
  • 4044 Kit Label Z019733-0019L
  • 4045 Kit Label 019733-0020L
  • INGREDIENTS AND APPEARANCE
    4044 FIRST AID KIT 
    4044 first aid kit kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4044
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-4044-01 1 in 1 KIT; Type 0: Not a Combination Product 11/21/2018
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 1 PACKET 0.9 g
    Part 2 6 POUCH 1.8 mL
    Part 3 4 PACKET 3.6 g
    Part 1 of 3
    NEOMYCIN 
    antibiotic ointment
    Product Information
    Item Code (Source) NDC:0498-0730
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0730-01 0.9 g 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 final part333B 03/31/2010
    Part 2 of 3
    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
    NONOXYNOL-9 (UNII: 48Q180SH9T)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0121-34 10 in 1 CARTON
    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 3 of 3
    FIRST AID BURN 
    benzalkonium chloride, lidocaine hydrochloride cream
    Product Information
    Item Code (Source) NDC:0498-0903
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 0.9 g 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 part333A 12/20/2017
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 11/21/2018
    4045 FIRST AID KIT 
    4045 first aid kit kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4045
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-4045-01 1 in 1 KIT; Type 0: Not a Combination Product 11/21/2018
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 4 PACKET 3.6 g
    Part 2 6 POUCH 1.8 mL
    Part 3 4 PACKET 3.6 g
    Part 1 of 3
    NEOMYCIN 
    antibiotic ointment
    Product Information
    Item Code (Source) NDC:0498-0730
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0730-01 0.9 g 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 final part333B 03/31/2010
    Part 2 of 3
    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
    NONOXYNOL-9 (UNII: 48Q180SH9T)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0121-34 10 in 1 CARTON
    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 3 of 3
    FIRST AID BURN 
    benzalkonium chloride, lidocaine hydrochloride cream
    Product Information
    Item Code (Source) NDC:0498-0903
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE 0.5 g  in 100 g
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0903-34 10 in 1 BOX, UNIT-DOSE
    1 0.9 g 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 part333A 12/20/2017
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 11/21/2018
    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(0498-4044, 0498-4045)
    Establishment
    Name Address ID/FEI Business Operations
    Water-Jel Technologies 155522589 manufacture(0498-0903, 0498-0730)
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