Label: 4129 FIRST AID KIT kit
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NDC Code(s):
0498-0011-77,
0498-0121-00,
0498-0143-04,
0498-0501-00, view more0498-0733-00, 0498-0800-34, 0498-3334-00, 0498-4129-01
- 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 23, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Ammonia Active ingredient
- Ammonia Purpose
- Ammonia Uses
- Ammonia Warnings
- Ammonia Directions
- Ammonia Other information
- Ammonia Inactive ingredient
- Ammonia Questions or Comments?
- Pyrocaine Active ingredient
- Pyrocaine Purpose
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Pyrocaine
Uses
For the temporary relief of pain and itching, and to help protect against skin infection in:
- minor burns
- minor skin irritations
- minor cuts and scrapes
- insect bites
- sunburns
- Pyrocaine Warnings
- Pyrocaine Directions
- Pyrocaine Other information
- Pyrocaine Inactive ingredients
- PVP Active ingredient
- PVP Purpose
- PVP Uses
- PVP Warnings
- PVP Directions
- PVP Other information
- PVP Inactive ingredients
- PVP Questions
- Sting Relief Active ingredient (in each wipe)
- Sting Relief Purpose
- Sting Relef 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 Inactive ingredient
- Alcojol Questions
- Hydrocortisone Active ingredient (in each gram)
- Hydrocortisone Purpose
- Hydrocortisone Uses
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Hydrocortisone
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?
- BZK Active ingredient
- BZK Purpose
- BZK Uses
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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
- BZK Directions
- BZK Other information
- BZK Inactive ingredient
- BZK Questions
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4129
SF00004226 Kit Contents
1 AMMONIA INHALANTS 10 PER
1 EYE DRESS PKT W/4 ADH STRIPS
1 TRIANGULAR BDG, NON-STERILE
1 INSTANT COLD PACK 4" X 6"
1 ALCOHOL PREP PADS 10P
1 HYDROCORTISON,1.O%,1/32 OZ,10P
1 RESPONSE KIT BLOODBORNE PATHOG
1 SCISSOR BDGE 4" RED PLS HDL
1 BANDAGE COMP 2" W/TELFA PAD 4
1 BANDAGE COMP 4" W/TELFA PAD 1
LBL STOCK 6-3/8"X4"
LBL STOCK 4"X2-7/8"
1 LBL STOCK 3"x1-7/8"
1 PR LRG NITRILE GLVES ZIP BAG
1 1" X 3" PLASTIC BANDS 16/BAG
1 KIT STL 24 UN WHITE 01
1 PVP IODINE SWABS 10
1 STING Relief SWAB 10
1 PYRO-CAINE AERO 2/BX
1 RED BIO BAGS 2/BX
1 FACE MASK/EYE SHIELD
1 LIQD TRTMNT SYS 1 EA
1 DISP. TOWEL/WIPES 2EA
1 IMPERVIOUS GOWN 1 EA
- Ammonia Principal Display Panel
- Pyrocaine Principal Display Panel
- PVP Principal Display Panel
- Sting Relief Principal Display Panel
- Alcohol Principal Display Panel
- Hydrocortisone Principal Display Panel
- BZK Principal Display Panel
- 4129 Kit Label SF00004226
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INGREDIENTS AND APPEARANCE
4129 FIRST AID KITÂ
4129 first aid kit kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4129 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-4129-01 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 10 AMPULE 3 mL Part 3 2 CAN 28.4 g Part 4 10 POUCH 4 mL Part 5 10 POUCH 3 mL Part 6 4 PACKET 5.6 mL Part 7 10 POUCH 4 mL Part 8 10 PACKET 9 g Part 1 of 8 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 LIGHT MINERAL OIL (UNII: N6K5787QVP)  CETYL ALCOHOL (UNII: 936JST6JCN)  METHYLPARABEN (UNII: A2I8C7HI9T)  EDETATE DISODIUM (UNII: 7FLD91C86K)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  TROLAMINE (UNII: 9O3K93S3TK)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  WATER (UNII: 059QF0KO0R)  POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  STEARIC ACID (UNII: 4ELV7Z65AP)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  GLYCERIN (UNII: PDC6A3C0OX)  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 part348 03/06/2013 Part 2 of 8 AMMONIA INHALENTÂ
ammonia inhalent inhalantProduct Information Item Code (Source) NDC:0498-3334 Route of Administration RESPIRATORY (INHALATION) Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA 0.045 g  in 0.3 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-3334-00 0.3 mL in 1 AMPULE; 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 8 PYROCAINE BURNÂ
benzocaine, benzethonium chloride aerosol, sprayProduct Information Item Code (Source) NDC:0498-0011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 20 g  in 100 g BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.2 g  in 100 g Inactive Ingredients Ingredient Name Strength 1,1,3-TRI(3-TERT-BUTYL-4-HYDROXY-6-METHYLPHENYL)BUTANE (UNII: BF6E9O0XJN)  ISOBUTANE (UNII: BXR49TP611)  1,1,3-TRIS(2-CHLOROETHOXY)PROPANE (UNII: 4FEX9N888E)  DIPROPYLENE GLYCOL (UNII: E107L85C40)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0011-77 14.2 g in 1 CAN; 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 01/01/2018 Part 4 of 8 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 WATER (UNII: 059QF0KO0R)  MENTHOL (UNII: L7T10EIP3A)  BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  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 8 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 6 of 8 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 Part 7 of 8 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 OTC monograph not final part333A 09/18/2018 Part 8 of 8 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 LIGHT MINERAL OIL (UNII: N6K5787QVP)  CETYL ALCOHOL (UNII: 936JST6JCN)  METHYLPARABEN (UNII: A2I8C7HI9T)  EDETATE DISODIUM (UNII: 7FLD91C86K)  GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  TROLAMINE (UNII: 9O3K93S3TK)  PROPYLPARABEN (UNII: Z8IX2SC1OH)  WATER (UNII: 059QF0KO0R)  POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  STEARIC ACID (UNII: 4ELV7Z65AP)  DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  GLYCERIN (UNII: PDC6A3C0OX)  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0800-34 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 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 (079287321)