Label: 4298 FIRST AID KIT kit
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NDC Code(s):
0498-0100-01,
0498-0501-00,
0498-0730-01,
0498-0733-00, view more0498-0800-35, 0498-0801-35, 0498-4298-01
- 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 December 30, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Eyewash Active ingredient
- Eyewash 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.
- Eyewash Directions
- Eyewash Inactive ingredients
- Eyewash Questions
- Sting Relief Active ingredient (in each wipe)
- Sting Relief Purpose
- Sting Relief Uses
- Sting Relief Warnings
- Sting Relief Directions
- Sting Relief Inactive ingredients
- Questions or Comments?
- Hydrocortisone Cream Active ingredient (in each gram)
- Hydrocortisone Purpose
- Hydrocortisone Uses
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Hysrocortisone
Warnings
For external use only
When using the product
- avoid contact with eyes
- do not begin use of any other hydrocortisone product unless you have consulted a doctor
- do not use for the treatment of diaper rash
- Hydrocortisone Directions
- Hydrocortisone Other information
- Hydrocortisone Inactive ingredients
- Hydrocortisone Questions or Comments?
- Neomycin Active ingredient
- Neomycin Purpose
- Neomycin Uses
- Neomycin Warnings
- Neomycin Directions
- Neomycin Other information
- Neomycin Inactive ingredient
- Neomycin Questions
- BZK Active ingredient
- BZK Purpose
- BZK Uses
- BZK Warnings
- Keep out of reach of children
- BZ Directions
- BZK Other information
- BZK Inactive ingredient
- BZK Questions
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4298
011011-4165N Kit Contents
1 FNGRTIP-5 PER, KNCKL BDG-4 PER
1 NEOMYCIN ANTIBIOTIC 10 PER
3 TRIANGULAR BDG, NON-STERILE
1 BANDAGE COMP, 3" OFFSET, 2 PER
2 ADHESIVE BDG,PLSTIC,1"X3"16PER
1 ADH BAND, EXTRA LARGE, 6 PER
1 1 OZ EYE WASH W/PADS & STRIPS
1 HYDROCORTISON,1.O%,1/32 OZ,10P
1 BIOHAZARD BAG/SCRAPER BBP
1 ANTIMCRBL ANTSPTC TWLETTS 6PER
4 NITRILE GLOVES BBP
1 CPR MICROSHIELD W/2 PR LTX GLV
1 BBP PROTECT APPAREL KIT
LBL STOCK 6-3/8"X4"
1 LBL STOCK 3"x1-7/8"
1 KIT STL 24 UN WHITE 01
1 LABL FILL 24UN SOUTH CO ID F
1 STING RELIEF 10
- Eyewash Principal Display Panel
- Sting Relief Principal Display Panel
- Hydrocortisone Principal Display Panel
- Neomycin Principal Display Panel
- BZK Principal Display Panel
- 4298 Kit Label 011011-4165N
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INGREDIENTS AND APPEARANCE
4298 FIRST AID KITÂ
4298 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4298 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4298-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 10 PACKET 9 g Part 2 1 BOTTLE 30 mL Part 3 10 PACKET 9 g Part 4 10 POUCH 4 mL Part 5 10 PACKET 9 g Part 6 15 PACKET 21 mL Part 1 of 6 HYDROCORTISONEÂ
anti-itch creamProduct Information Item Code (Source) NDC:0498-0801 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE ACETATE 1 g  in 100 g Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  STEARIC ACID (UNII: 4ELV7Z65AP)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  CETYL ALCOHOL (UNII: 936JST6JCN)  TROLAMINE (UNII: 9O3K93S3TK)  METHYLPARABEN (UNII: A2I8C7HI9T)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  GLYCERIN (UNII: PDC6A3C0OX)  WATER (UNII: 059QF0KO0R)  CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0801-35 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 OTC monograph not final part348 10/15/2019 Part 2 of 6 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, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  SODIUM CHLORIDE (UNII: 451W47IQ8X)  SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  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 3 of 6 NEOMYCINÂ
antibiotic ointmentProduct 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 4 of 6 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 ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.5 mL  in 1 mL LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 20 mg  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 5 of 6 HYDROCORTISONEÂ
anti-itch cream ointmentProduct Information Item Code (Source) NDC:0498-0800 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE ACETATE 1 g  in 100 g Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  LIGHT MINERAL OIL (UNII: N6K5787QVP)  STEARIC ACID (UNII: 4ELV7Z65AP)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  CETYL ALCOHOL (UNII: 936JST6JCN)  TROLAMINE (UNII: 9O3K93S3TK)  METHYLPARABEN (UNII: A2I8C7HI9T)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  GLYCERIN (UNII: PDC6A3C0OX)  WATER (UNII: 059QF0KO0R)  CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  EDETATE DISODIUM (UNII: 7FLD91C86K)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0800-35 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 OTC monograph not final part348 03/06/2013 10/15/2019 Part 6 of 6 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 OTC monograph not final part333E 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/18/2018 Labeler - Honeywell Safety Products USA, INC (118768815)