Label: 4229 FIRST AID KIT- 4229 first aid kit

  • NDC Code(s): 0498-0143-04, 0498-0750-36, 0498-2422-01, 0498-3334-00, view more
    0498-4229-01
  • 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 March 23, 2019

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

  • Ammonia Inhalent Active ingredient

    Ammonia 15%

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  • Ammonia Inhalent Purpose

    Respiratory stimulant

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  • Ammonia Inhalent Uses

    • to prevent or tret fainting
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  • Ammonia Inhalent Warnings

    For external use only

    Do not use

    • if you have breathing problems such as asthma or emphysema

    Stop use and ask a doctor if

    • condition persists

    Keep out of reach of children

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

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  • Ammonia Inhalent Directions

    • hold inhalant away from face and crush ampoule between thumb and forefinger at position indicated on sleeve.
    • hold near nostrils for inhalation of volatile vapor
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  • Ammonia Inhalent Other information

    • store at room temperature away from light
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  • Ammonia Inhalent Other information

    • store at room temperature away from light
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  • Ammonia Inhalent Inactive ingredients

    alcohol USP, FD&C red #40, lavender oil, lemon oil fcc, nutmeg oil, purified water

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  • Ammonia Inhalent Questions or Comments

    1-800-430-5490

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  • Alcohol Wipe Active ingredient

    Isopropyl alcohol 70%

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  • Alcohol Wipe Purpose

    First aid antiseptic

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  • Alcohol Wipe Uses

    • first aid to help prevent infection in minor cuts, scrapes, and burns
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  • Alcohol Wipe Warnings

    For external use only

    Do not use

    • in the eyes
    • over large areas of the body


    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burn


    When using this product

    • do not use longer than one week unless directed by a doctor


    Stop use and consult a doctor

    • if 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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  • Alcohol Wipe Directions

    • clean the affected area
    • apply wipe to affected area 1 to 3 times daily
    • may be covered with a sterile bandage
    • discard wipe after single use
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  • Alcohol Wipe Other information

    store at room temperature 15 0 to 25 0 C (59 0 to 77 0F)

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  • Alcohol Wipe Inactive ingredient

    water

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  • Alcohol Wipe Questions

    1-800-430-5490

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  • Aypanal Active ingredient

    Acetaminophen 325 mg

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  • Aypanal Purpose

    Pain reliever/ fever reducer

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  • Aypanaly Uses

    • temporarily relieves minor aches and pains due to the common cold and headache - temporarily reduces fever

    Keep out of reach of children.

    Keep out of reach of children.

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  • Aypanal Warnings

    Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:

    • more than 4,000 mg in 24 hours, which is the maximum daily amount
    • child takes more than 5 doses in 24 hours, which is the maximum daily amount
    • taken with other drugs containing acetaminophen
    • adult has 3 or more alcoholic drinks every day while using this product:

    Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

    • skin reddening
    • blisters
    • rash
    • If a skin rash occurs, stop use and seek medical help right away.

    Do not use

    • with any other drug containing acetaminophen (prescription or nonprescription).
    • If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

    Ask a doctor before use if you have

    • liver disease


    Ask a doctor or pharmacist before use if

    • you are taking the blood thinning drug warfarin


    Stop using and ask a doctor if

    • pain gets worse or lasts more than 10 days in adults
    • pain gets worse or lasts more than 5 days in children under 12 years
    • fever gets worse or lasts more than 3 days
    • redness or swelling is present
    • new symptoms occur

    If pregnant or breast-feeding

    If pregnant or breast-feeding, ask a health professional before use.


    Overdose warning

    • In case of accidental overdose, get medical help or contact a Poison Control Center right away.
    • Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
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  • Aypanal Directions

    do not take more than directed (see overdose warning)

    ​adults and children 12 years of age or older

    • take two tablets every 4-6 hours while symptoms last
    • do not take more than 12 tablets in 24 hours

    children 6 to under 12 years of age

    • take 1 tablet every 4-6 hours while symptoms last
    • do not take more than 5 tablets in 24 hours

    children under 6 years consult a doctor

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  • Aypanal Other information

    • store at room temperature 15 0 to 30 0 C (59 0 - 86 0 F)
    • TAMPER EVIDENT PACKETS- DO NOT USE IF OPEN OR TORN
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  • Aypanal Inactive ingredients

    corn starch, microcrystalline cellulose, povidone, sodium starch glycolate, stearic acid

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  • Aypanal Questions

    1-800-430-5490

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  • Triple Active ingredient

    Bacitracin zinc 400 units

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

    Polymyxin B sulfate 5000 units

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  • Triple Purpose

    First aid antibiotic

    First aid antibiotic -

    First aid antibiotic

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  • Triple Uses

    first aid to help prevent infection in

    • minor cuts
    • scrapes -
    • burns
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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

    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

    Ask a doctor before use if you have

    • a deep or puncture wounds
    • animal bites
    • serious burns

    Keep out of the reach of children

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

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  • Triple 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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  • Triple Other information

    • store at 15 o to 25 oC (59 o to 77 o F)
    • tamper evident sealed packets
    • do not use if packet is torn or opened
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  • Triple Inactive ingredient

    petrolatum

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  • Pain Stoppers Active ingredient

    Acetaminophen 110mg

    Aspirin 162mg (NSAID)*

    Caffeine 32.4mg

    Salicylamide 152mg (NSAID)*

    *nonsteroidal anti-inflammatory drug

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  • Pain Stoppers Purpose

    Pain reliever/fever reducer

    Pain reliever/fever reducer

    Diuretic

    Pain reliever/fever reducer

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  • Pain Stoppers Uses

    for the temporary relief of minor aches and pains due to:

    • common cold

    • headache

    • muscular aches

    • premenstrual and menstrual cramps

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  • Pain Stoppers Warnings

    Reye's syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

    Allergy alert: Aspirin may cause a severe allergic reaction which may include:

    • hives
    • facial swelling
    • asthma (wheezing)
    • shock

    Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

    • skin reddening
    • blisters
    • rash

    If skin reaction occurs, stop use and seek medical help right away.

    Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:

    more than 12 tablets in 24 hours, which is the maximum daily amount
    with other drugs containing acetaminophen
    3 or more alcoholic drinks every day while using this product

    Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you:

    • are age 60 or older
    • have had stomach ulcers or bleeding problems
    • take a blood thinning (anticoagulant) or steroid drug
    • take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen or others)
    • have 3 or more alcoholic drinks every day while using this product
    • take more or for a longer time than directed

    Do not use

    • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist
    • for more than 10 days for pain unless directed by a doctor
    • for more than 3 days for fever unless directed by a doctor

    Ask a doctor before use if

    • stomach bleeding warning applies to you
    • you have a history of stomach problems, such as heartburn
    • you are taking a diuretic
    • you have high blood pressure, heart disease, liver cirrhosis, or kidney disease

    Stop use and ask a doctor if

    • symptoms do not improve
    • new symptoms occur
    • pain or fever persists or gets worse
    • you experience any of the following signs of stomach bleeding:
    • feel faint
    • vomit blood
    • have bloody or black stools
    • have stomach pin that does not get better
    • if ringing in the ears or a loss of hearing occurs, consult a doctor before taking any more of this product.

    If pregnant or breast-feeding

    • ask a healthcare professional before use.

    It is especially important not to use aspirin during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during pregnancy.

    Keep out of reach of children

    Overdose warning : In case of accidental overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

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  • Pain Stoppers Directions

    • adults and children 12 years of age and over, take 2 tablets every 4 hours while symptoms persist
    • do not take more than 12 tablets in 24 hours
    • children under 12 years: consult a doctor

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  • Pain Stoppers Other information

    store at a controlled room temperature 15 0 -30 0 C (59 0 -86 0 F)
    TAMPER EVIDENT-DO NOT USE IF OPEN OR TORN

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  • Pain Stoppers Inactive ingredients

    FD&C Yellow #6, magnesium stearate, microcrystalline cellulose, povidone, starch, stearic acid,

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  • Pain Stoppers Questions or Comments?

    1-800-430-5490

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  • 4229 68140FEDX Kit Contents

    1 WOVEN 2" X 3" 25/BOX

    1 FINGERTIP "T" WOVEN 40/BOX

    1 1X3 WOVEN SING 50/BOX

    1 SWIFT KNUCKLE 40/BX

    1 AMMONIA INHALANTS 10 PER

    1 NITRILE GLOVES 2PR BBP

    1 ADHESIVE TAPE W/P 1" X 10YDS

    1 GAUZE BANDAGE 2"X2 YDS STRETCH GZ

    1 FIRST AID GUIDE ASHI

    1 BLOODSTOPPER

    1 CTA STRL 6" SGL TIP 12/2

    1 ALCOHOL WIPES 50'S

    1 AYPANAL NON-ASP IND 2/ENV 100

    1 PAIN STOPPERS IND PK 2ENV 250

    1 TRIPLE BIOTIC .5 GRAM PKT 20

    1 SCISSOR BDGE 4" RED PLS HDL

    1 KIT TWEEZER 3 1/2" SLANTED

    1 F A KIT EMPTY BLANK 140

    LBL STOCK 6-3/8"X4"

    1 LBL STOCK 3"x1-7/8"

    1 TRI BNDG NON WOVEN 40"X40"X56"

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  • Ammonia inhalent Principal Display Panel
  • Alcohol Wipe Principal Display Panel
  • Aypanal Principal Display Panel
  • Triple Principal Display Panel
  • Pain Stoppers Principal Display Panel
  • 4229 Kit Label 68410FEDX
  • INGREDIENTS AND APPEARANCE
    4229 FIRST AID KIT 
    4229 first aid kit kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4229
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-4229-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 20 PACKET 10 g
    Part 2 125 PACKET 250 
    Part 3 10 AMPULE 3 mL
    Part 4 50 POUCH 20 mL
    Part 5 50 PACKET 100 
    Part 1 of 5
    TRIPLE ANTIBIOTIC 
    bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment
    Product 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
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 3.5 mg  in 1 g
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [iU]  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:0498-0750-36 0.5 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
    OTC monograph final part333B 09/19/2018
    Part 2 of 5
    PAIN STOPPERS 
    acetaminophen, caffeine, aspirin, salicylamide tablet
    Product Information
    Item Code (Source) NDC:0498-2422
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 110 mg
    ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 162 mg
    CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE 32.4 mg
    SALICYLAMIDE (UNII: EM8BM710ZC) (SALICYLAMIDE - UNII:EM8BM710ZC) SALICYLAMIDE 152 mg
    Inactive Ingredients
    Ingredient Name Strength
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POVIDONE K30 (UNII: U725QWY32X)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    Product Characteristics
    Color orange (Bright Orange) Score no score
    Shape ROUND Size 11mm
    Flavor Imprint Code FR;2
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-2422-01 2 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 part343 01/02/2017
    Part 3 of 5
    AMMONIA INHALENT 
    ammonia inhalent inhalant
    Product 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 4 of 5
    ALCOHOL WIPE 
    isopropyl alcohol swab
    Product 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 5 of 5
    AYPANAL NON-ASPIRIN 
    acetaminophen tablet
    Product Information
    Item Code (Source) NDC:0498-2001
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
    Inactive Ingredients
    Ingredient Name Strength
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    POVIDONE (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    Product Characteristics
    Color white Score 2 pieces
    Shape ROUND Size 10mm
    Flavor Imprint Code circle;U
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 2 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 part343 04/10/2012
    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)
    Establishment
    Name Address ID/FEI Business Operations
    James Alexander 040756421 manufacture(0498-3334)
    Establishment
    Name Address ID/FEI Business Operations
    Honeywell Safety Products USA, INC 079287321 pack(0498-4229)
    Establishment
    Name Address ID/FEI Business Operations
    Ultra Seal Corporation 085752004 manufacture(0498-2001, 0498-2422)
    Establishment
    Name Address ID/FEI Business Operations
    Water-Jel Technologies 155522589 manufacture(0498-0750)
    Establishment
    Name Address ID/FEI Business Operations
    Changzhou Maokang Medical 421317073 manufacture(0498-0143)
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