Label: 4239 FIRST AID KIT- 4239 first aid kit
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NDC Code(s):
0498-0100-01,
0498-0121-00,
0498-0143-04,
0498-0203-00, view more0498-0501-00, 0498-0733-00, 0498-0750-35, 0498-4239-01
- Packager: Honeywell Safety Products USA, Inc.
- Category: HUMAN OTC DRUG LABEL
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 January 22, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Burn Jel Active ingredient
- Burn Jel Purpose
- Burn Jel Uses
- Burn Jel Warnings
- Burn JEl Directions
- Burn Jel Other information
- Burn Jel Inactive ingredients
- Burn Jel Questions
- Triple Active ingredient
- Triple Purpose
- Triple Uses
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Triple
Warnings
For external use only
Allergy alert: do not use if you are allergic to any of the ingredients
Do not use
- in the eyes
- over large areas of the body
- Ask a doctor before use if you have
- a deep or puncture wounds
- animal bites
- serious burns
- Triple Directions
- Triple Other information
- Triple Inactive ingredient
- Triple Questions?
- BZK Wipe Active ingredient
- BZK Wipe Purpose
- BzK Wipe Uses
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BZK Wipe
Warnings
For external use onlyDo 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
- BZK Wipe Directions
- BZK Wipe Other information
- BZK Wipe Inactive ingredient
- BZK Wipe Questions
- Sting Relief Active ingredient (in each wipe)
- Sting Relief Purposse
- Sting Relief Uses
- Sting Relief Warnings
- Sting Relief Directions
- Sting Relief Inactive ingredients
- Sting Relief Questions or Comments?
- Alcohol Active ingredient
- Alcohol Purpose
- Alcohol Uses
- Alcohol Warnings
- Alcohol Directions
- Alcohol Other information
- Alcohol Questions
- Eyewash Active ingredient
- Eyewassh Purpose
- Eyewash Uses
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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.
- Eyeash Directions
- Eyewash Inactive ingredients
- Eyeash Questions
- PVP Wipe Active ingredient
- PVP Wipe Purpose
- PVP Wipe Uses
- PVP Wipe Warnings
- PVP Wipe Directions
- PVP Wipe Other information
- PVP Wipe Inactive ingredients
- PVP Wipe Questions
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4239
013111-4536 kit contents
1 KNUCKLE BAND 8 PER
1 TRIPLE ANTIBIOTIC 10 PER
1 EYE DRESS PKT W/4 ADH STRIPS
1 TRIANGULAR BDG, NON-STERILE
1 ADH TAPE, .5" X 2.5 YD, 2 PER
1 GAUZE PADS, 4" X 4", 2 PER
1 GAUZE COMP, 1 SQ YARD, 1 PER
1 BUFFERED EYE WASH 1 OZ BTL
1 BANDAGE COMP, 2" OFFSET, 4 PER
1 BANDAGE COMP, 4" OFFSET, 1 PER
1 ADHESIVE BDG,PLSTIC,1"X3"16PER
1 ADH BAND, EXTRA LARGE, 6 PER
1 BURN JEL 1/8 OZ, 6 PER
1 WATER JEL DRESSING 4" X 4"
1 PVP IODINE WIPES 10 PER
1 BIOHAZARD BAG,WIPES/TOWELS BBP
1 FACE MASK W/SHIELD 1 PER BBP
1 NITRILE GLOVES 2PR BBP
1 FIRST AID GUIDE ASHI
1 MICROSHIELD W/VNL GLV/ALCL
LBL STOCK 6-3/8"X4"
LBL STOCK 4"X2-7/8"
1 LBL STOCK 3"x1-7/8"
1 LABEL NORTH CONTENTS 8X8 ID B
1 KIT PP 24 UNIT FA
1 STING Relief WIPES 10
- Burn Jel Principal Display Panel
- Triple Principal Display Panel
- BZK Wipe Principal Display Panel
- Sting Relief Principal Display Panel
- Alcohol Principal Display Panel
- Eyewash Principal Display Panel
- PVP Wipe Principal Display Panel
- 4239 Kit Label 013111-4536
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INGREDIENTS AND APPEARANCE
4239 FIRST AID KITÂ
4239 first aid kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4239 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4239-01 1 in 1 KIT 09/13/2018 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 6 PACKET 21 g Part 2 10 POUCH 3 mL Part 3 1 BOTTLE 30 mL Part 4 10 PACKET 9 g Part 5 2 PACKET 2.8 mL Part 6 4 POUCH 1.6 mL Part 7 10 POUCH 4 mL Part 1 of 7 BURN JELÂ
gel for burns gelProduct Information Item Code (Source) NDC:0498-0203 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 2 g  in 100 g Inactive Ingredients Ingredient Name Strength TEA TREE OIL (UNII: VIF565UC2G)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  METHYLPARABEN (UNII: A2I8C7HI9T)  EDETATE DISODIUM (UNII: 7FLD91C86K)  GLYCERIN (UNII: PDC6A3C0OX)  TROLAMINE (UNII: 9O3K93S3TK)  CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: HHT01ZNK31)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  OCTOXYNOL-9 (UNII: 7JPC6Y25QS)  DIPROPYLENE GLYCOL (UNII: E107L85C40)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0203-00 3.5 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 unapproved drug other 09/19/2018 Part 2 of 7 PVP IODINE WIPEÂ
povidone-iodine 10% swabProduct 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:0498-0121-00 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 7 EYESALINE EMERGENCY EYEWASHÂ
purified water liquidProduct 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 Drug M018 12/18/2018 Part 4 of 7 TRIPLE ANTIBIOTICÂ
bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointmentProduct Information Item Code (Source) NDC:0498-0750 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 5000 [iU]  in 1 g BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [iU]  in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 3.5 mg  in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U)  Product Characteristics Color white Score     Shape Size Flavor Imprint Code Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0750-35 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 unapproved drug other 09/19/2018 Part 5 of 7 ANTISEPTIC TOWELETTEÂ
benzalkonium chloride liquidProduct 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 unapproved drug other 12/22/2017 Part 6 of 7 ALCOHOL WIPEÂ
isopropyl alcohol swabProduct Information Item Code (Source) NDC:0498-0143 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.7 mL  in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0143-04 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 unapproved drug other 09/18/2018 Part 7 of 7 STING RELIEF PADÂ
ethyl alcohol, lidocaine swabProduct 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 unapproved drug other 12/23/2017 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. (118768815)