Label: 4248 FIRST AID KIT- 4248 first aid kit

  • NDC Code(s): 0498-0021-40, 0498-0031-40, 0498-0100-02, 0498-0143-04, view more
    0498-0501-00, 0498-0733-00, 0498-0750-36, 0498-0800-35, 0498-2422-01, 0498-3334-00, 0498-4248-01
  • 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 May 22, 2019

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

  • Eyewash Active ingredient

    Sterile Water 99%

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  • Eyewash Purpose

    Eyewash

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  • Eyewash Uses

    • for flushing the eye to remove loose foreign material, air pollutants or chlorinated water
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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.

    Stop use and ask a doctor if

    • you experience eye pain
    • changes in vision
    • continued redness or irritation of the eye
    • condition worsens or persists

    Keep out of reach of children

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

    • remove contacts before using
    • twist top to remove
    • flush the affected area as needed
    • control rate of flow by pressure on the bottle
    • if necessary, continue flushing with emergency eyewash or shower
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  • Eyewash Inactive ingredients

    sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

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  • Eyewash Questions

    1-800-430-5490

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  • Ammonia Active ingredient

    Ammonia 15%

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  • Ammonia Purpose

    Respiratory stimulant

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  • Ammonia Uses

    • to prevent or treat fainting
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  • Ammonia 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 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 Other information

    • store at room temperature away from light
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  • Ammonia Inactive ingredient

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

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  • Ammonia Questions or Comments?

    1-800-430-5490

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  • Water Soluble 1st Aid Spray Active ingredient

    Benzethonium chloride 0.2% w/w - Benzocaine 10% w/w

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  • Water Soluble 1st Aid Spray Purpose

    Topical antiseptic

    Topical anesthetic

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  • Water Soluble 1st Aid Spray Uses

    for temporary relief of pain and itching and helps protect against infection in

    • minor cuts and scrapes
    • insect bites
    • minor skin irritations

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  • Water Soluble 1st Aid Spray Warnings

    For external use only

    Flammable

    • keep away from fire or flame
    • contents under pressure
    • do not puncture or incinerate container
    • do not expose to temperature above 120 0 F

    Do not use

    • in the eyes or other mucous membranes
    • in cases of serious burns
    • in case of deep orpuncture wounds
    • for a prolonged period of time
    • on large portion of the body


    Stop use and ask a doctor if

    • condition worsens or symptoms persist for more than 7 days
    • condition clears up and occurs again within a few days
    • redness, swelling, or irritation occurs

    Keep out of reach of children

    • If swallowed, get medical help or contact a Poison Control Center right away
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  • Water Soluble 1st Aid Spray Directions

    • clean the affected area
    • shake can well before using
    • hold 4 - 6 inches from surface and spray area until wet
    • may be covered with a sterile bandage. If bandaged, let dry first
    • for adult institutional use only
    • not intended for use on children
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  • Water Soluble 1st Aid Spray Other information

    • avoid inhaling
    • use only as directed
    • intentional misuse by deliberately concentrating and inhaling the contents may be harmful or fatal
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  • Water Soluble 1st Aid Spray Inactive ingredients


    dipropylene glycol, isobutane, N-butane, propane

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  • Burn Relief Water Soluble Active ingredients

    Benzethonium chloride 0.2% w/w

    Benzocaine 10% w/w

    Menthol 0.33% w/w

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  • Burn Relief Water Soluble Purpose


    Topical antiseptic

    Topical anesthetic

    Topical anesthetic

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  • Burn Relief Water Soluble Uses

    for the temporary relief of pain and itching and helps protect against infection in:

    • minor cuts and scrapes
    • burns
    • sunburn
    • insect bites
    • minor skin irritations
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  • Burn Relief Water Soluble Warnings

    For external use only

    Flammable keep away from fire or flame

    • contents under pressure
    • do not puncture or incinerate container
    • do not expose to temperatures above 120 0 F

    Do not use

    • in or near the eyes or other mucous membranes
    • in case of serious burns
    • in case of deep or puncture wounds
    • for prolonged period of time
    • on large portion of the body

    Stop use and ask a doctor if

    • condition worsens or symptoms persist for more than 7 days
    • condition clears up and recurs within a few days
    • redness, swelling, or irritation occurs

    Keep out of the reach of children

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

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  • Burn Relief Water Soluble Directions

    • clean the affected area
    • shake can well before using
    • hold 4 - 6 inches from surface and spray area until wet
    • may be covered with a sterile bandage, if bandaged let dry first
    • for adult institutional use only
    • not intended for use on children
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  • Burn Relief Water Soluble Other information

    • avoid inhaling
    • use only as directed
    • intentional misuse by deliberately concentrating or inhaling the contents may be harmful or fatal
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  • Burn Relief Water Soluble Inactive ingredients

    dipropylene glycol, isobutane, n-butane, propane

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  • Triple Active ingredients

    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

    Ask a doctor before use if you have

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


    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

    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 0 to 25 0 C (59 0 to 77 0 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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  • Alcohol Active ingredient

    Isopropyl alcohol 70%

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  • Alcohol Purpose

    First aid antiseptic

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  • Alcohol Uses

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

    For external use only

    Flammable, keep away from fire or flame.

    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 burns

    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 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 Other information

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

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  • Alcohol Inactive ingredient

    water

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  • Miralac Active ingredient (in each chewable tablet)
  • Miralac Purpose

    Antacid

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  • Miralac Uses

    for the relief of

    • acid indigestion
    • heartburn
    • sour stomach
    • upset stomach associated with these symptoms
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  • Warnings

    Ask a doctor before use if you have

    • kidney stones
    • calcium-restricted diet

    Ask a doctor before use if you are

    • presently taking a prescription drug. Antacids may interfere with certain prescription drugs

    When using this product

    • do not take more than 12 tablets in a 24- hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

    Keep out of the reach of children.

    In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

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  • Miralac Directions

    • chew 1 to 2 tablets every 4 hours as symptoms occur, or as directed by a doctor.
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  • Miralac Other information

    • each tablet contains: calcium 170 mg
    • sucrose free
    • lactose free
    • store at room temperature
    • TAMPER EVIDENT PACKETS- DO NOT USE IF OPEN OR TORN
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  • Miralac Inactive ingredients

    magnesium stearate, mint flavor, silicon dioxide, sorbitol, starch

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  • Miralac Questions or comments?

    1-800-430-5490

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  • BZK Active ingredient

    Benzalkonium chloride 0.13% w/v

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  • BZK Purpose

    First aid antiseptic

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  • BZK Uses


    Antiseptic cleansing of face, hands, and body without soap and water

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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

    Stop use and ask a doctor if

    • if irritation, redness or other symptoms develop
    • the 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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  • BZK Directions


    tear open packet and use as a washcloth

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  • BZK Other information

    • store at room temperature 15 0 to 30 0 C (5 0 - 86 0 F)
    • do not reuse towelette
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  • BZK Inactiave ingredient

    water

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  • BzK Questions

    1-800-430-5490

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  • Aypanal Active ingredient

    Acetaminophen 500 mg

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  • Aypanal Purpose

    Pain reliever/fever reducer

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  • Aypanal Uses

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

    Ask a doctor before use if you have

    • liver disease
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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.
    • 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 skin reaction 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 or pharmacist before use if

    • you are taking the blood thinning drug warfarin

    Stop use and ask a doctor if

    • pain gets worse or lasts more than 10 days
    • fever gets worse or lasts more than 3 days
    • new symptoms occur
    • redness or swelling is present

    If pregnant or breastfeeding

    • ask a health professional before use.

    Keep out of reach of children.

    Keep out of reach of children.

    Overdose warning: In case ofl overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). 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 and over: Take 2 tablets with water every 6 hours while symptoms last.
    • do not take any more than 8 tablets in 24 hours.
    • children under 12: consult a doctor
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  • Aypanal Other information

    • store at 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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  • Aypanal Inactive igredients

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

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  • Aypanal Questions or Comments

    1-800-430-5490

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  • Hydrocortisone Active ingredient (in each gram)

    Hydrocortisone acetate (equivalent to Hydrocortisone 1%)

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  • Hyrdocortisone Purpose

    Anti-itch cream

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  • Hydrocortisone Uses

    • for the temporary relief of itching associated with minor skin irritations and rashes
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  • Hydrocortisone Warnings

    For external use only

    Ask a doctor before use if

    • you are using any other hydrocortisone product

    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

    Stop use and ask a doctor if

    • condition worsens
    • condition persists for more than 7 days
    • condition clears up and recurs within a few days

    Keep out of reach of children

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

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  • Hydrocortisone Directions

    • adults and children 2 years and older:
    • clean the affected area
    • apply to the area not more than 3 to 4 times daily
    • children under 2 years of age: consult a doctor
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  • Hydrocortisone Other information

    • store at room temperature (do not freeze)
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  • Hydrocortisone Inactive ingredients

    cetyl alcohol, citric acid, diazolidinyl urea, edetate disodium, glycerin, glyceryl monostearate, methylparaben, mineral oil, polyethylene glycol, propylene glycol, propylparaben, purified water, stearic acid, trolamine

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  • Hydrocortisone Questions or Comments?

    1-800-430-5490

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  • Sting Relief Active ingredient (in each wipe)

    Ethyl alcohol 50.0%

    Lidocaine HCl 2.0%

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  • Sting Relief Purpose

    Antiseptic

    Topical pain relief

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  • Sting Relief Uses

    • prevent infection in minor scrapes, and temporary relief of itching of insect bites

    Stop use and ask a doctor

    • if conditions worsen or persist for more than 7 days or clear up and occur again within a few days
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  • Sting Relief Warnings

    For external use only

    Flammable, keep away from open fire or flame

    Do not use

    • over large areas of the body
    • in eyes
    • over raw or blistered areas

    Keep out of reach of children.

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

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  • Sting Relief Directions

    • adults and children 2 years and older: Apply to cleaned affected area not more than 3 times daily.
    • children under 2 years of age: consult a doctor.
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  • Sting Relief Inactive ingredients

    benzalkonium chloride, menthol, and purified water

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  • Questions or Comments?

    1-800-430-5490

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  • Pain Stopper Active ingredient (in each tablet)

    Acetaminophen 110mg

    Aspirin 162mg (NSAID)*

    Caffeine 32.4mg

    Salicylamide 152mg (NSAID)*

    *nonsteroidal anti-inflammatory drug

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  • Pain Stopper Purpose

    Pain reliever/fever reducer

    Pain reliever/fever reducer

    Diuretic

    Pain reliever/fever reducer

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  • Pain Stopper 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 Stopper 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 using 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.

    Close
  • Pain Stopper 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 Stopper 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 Stopper Inactive ingredients

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

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  • Pain Stopper Questions or Comments?

    1-800-430-5490

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  • Sinus Decongestant Active ingredient (in each tablet)

    Acetaminophen 500 mg

    Phenylephrine HCl 5 mg

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  • Sinus Decongestant Purpose

    Pain relieve/fever reducer

    Nasal decongestant

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  • Sinus Decongestant Uses

    • temporarily relieves these symptoms associated with hayfever and other upper respiratory allergies
    • headache
    • sinus congestion and pressure
    • nasal congestion
    • minor aches and pains
    • helps decongest sinus openings and passages
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  • Sinus Decongestant Warnings

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

    • if you take more than 4,00 mg acetaminophen 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

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

    • skin reddening
    • blisters
    • rash

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

    Do not use

    • with any other product containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
    • if you are now taking a prescription monoamine oxidase inhibiter (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before use.

    Ask a doctor before use if you have

    • heart disease
    • high blood pressure
    • diabetes
    • thyroid disease
    • difficulty in urination due to enlargement of the prostate gland
    • liver disease

    Ask a doctor or pharmacist before use if you are

    • taking the blood thinning drug warfarin.

    Stop use and ask a doctor if

    • nervousness, dizziness or sleeplessness occur
    • pain or nasl congestion get worse or last more than 7 days
    • fever gets worse or lasts more than 3 days
    • new symptoms occur
    • redness or swelling is present

    If pregnant or breast-feeding

    • ask a health professional before use.

    Keep out of the reach of children.

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

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  • Sinus Decongestant Directions

    do not take more than directed (see overdose warning)

    Adults and children 12 years of age and older: take 2 tablets every 4-6 hours while symptoms persist

    • do not exceed 8 tablets in 24 hours unless directed by a doctor

    Children under 12 years: consult a doctor

    Close
  • Sinus Decongestant Other information

    • store at room temperature 15-30C (59-86F)
    • avoid excessive heat and humidity
    • TAMPER EVIDENT PACKETS - DO NOT USE IF OPEN OR TORN
    Close
  • Sinus Deacongestant Inactive ingredients

    FD&C Blue #1, microcrystalline cellulose, povidone, sodium starch glycolate, starch, stearic acid

    Close
  • Sinus Decongestant Questions or Comments?

    1-800-430-5490

    Close
  • Tetrahydrozoline HCL Active ingredient

    Tetrahydrozoline HCl 0.05%

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  • Tetrahydrozoline HCL Purpose

    Redness reliever

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  • Tetrahydroziline HCL Uses

    • relieves redness of the eye due to minor eye irritations
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  • Tetrahydrozoline HCL Warnings

    For external use only

    Do not use

    • if solution changes color or becomes cloudy

    Ask a doctor before use if

    • you have narrow angle glaucoma


    When using this product

    • pupils may become enlarged temporarily
    • overuse may produce increased redness of the eye
    • remove contact lenses before using
    • to avoid contamination, do not touch tip of container to any surface
    • replace cap after using

    Stop use and ask a doctor if

    • you experience eye pain, changes in vision, continued redness or irritation of the eye
    • the condition worsens or persists for more than 72 hours

    If pregnant or breast-feeding,

    • ask a health professional before use.

    Keep out of reach of children.

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

    Close
  • Tetrahydrozoline HCL Directions

    Instill 1 or 2 drops in the affected eye(s) up to four times daily.

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  • Tetrahydrozoline HCL Other information

    Store at 15° to 30°C (59° to 86°F)

    • Tamper evident. Do not use this product if imprinted neckband is missing or broken.
    • RETAIN THIS CARTON FOR FUTURE REFERENCE

    Distributed by

    North by Honeywell

    900 Douglas Pike

    Smithfield, RI 02917

    Close
  • Tetrahydrozoline HCL Inactive ingredients

    benzalkonium chloride, boric acid, edetate disodium, purified water, sodium borate, sodium chloride

    Close
  • 4248 68600PROAM KIT CONTENTS

    1 1X3 PLASTIC 100/BOX

    1 WOVEN 2" X 3" 25/BOX

    1 FINGERTIP 8 WOVEN 25/BOX

    1 FINGERTIP "T" WOVEN 40/BOX

    1 BUTTERFLY CLOS MED 100/BX DS

    1 SWIFT KNUCKLE 40/BX

    1 1 X 3 WOVEN 100/BOX

    1 AMMONIA INHALANTS 10 PER

    1 EYE DRESS PKT W/4 ADH STRIPS

    2 GAUZE BANDAGE, 4" X 6 YD

    1 INSTANT COLD PACK 4" X 6"

    1 HYDROCORTISON,1.O%,1/32 OZ,10P

    1 ELASTIC TAPE 1" X 5YD

    1 O/H TAPE ADHESIVE TRI-CUT

    2 GAUZE BANDAGE 1" x 2 YDS

    2 GAUZE BANDAGE 2"X2 YDS STRETCH GZ

    2 GAUZE BANDAGE 4"X2 YDS STRETCH GZ

    1 FIRST AID GUIDE ASHI

    2 BLOODSTOPPER

    1 NON ADHERENT PADS 2"X3" 50'S

    1 ABD COMBINE PAD 5" X 9"

    1 GZE PADS STERILE 4"X 4" 25'S

    1 CO-FLEX BANDAGE 2"X 5YDS TAN

    1 CPR FILTERSHIELD 77-100

    1 COTTON TIPS 100 PER VIAL

    1 ANTISEPTIC WIPES BZK CHL 20'S

    1 FIRST AID SPRAY AEROSOL 3 OZ

    1 ALCOHOL WIPES 50'S

    1 AYPANAL NON-ASP IND 2/ENV 250

    1 PAIN STOPPERS IND PK 2ENV 250

    1 MIRALAC TABS IND PK 2/ENV 250

    1 BURN SPRAY 3 OZ

    1 SINUS DECONGESTANT 2/ENV 100

    1 TRIPLE BIOTIC .5 GRAM PKT 20

    1 HYDROCORTISONE 1% .9 GRM 20'S

    1 TETRASINE EYE DROPS 1/2 OZ

    2 HAND & SKIN LOTION 1GM 20/BX

    1 SWIFT-STAT BLOOD CLOTTER 3 OZ

    1 COLD SPRAY 4 OZ

    1 POISON OAK/IVY CLEANSER 4 OZ

    1 COLD PACK 5"X9" BOXED

    2 4OZ BFS EYEWASH TRILINGUAL BOTTLE

    1 SPLINTER FORCEP 4 1/2"

    1 SCISSOR LISTER BDG S/S 5 1/2"

    1 POCKET INSERT RED #600 KIT

    1 600 EMPTY KIT BLANK

    1 LBL STOCK 6-3/8"X4"

    1 LBL STOCK 4"X2-7/8"

    1 LBL STOCK 3"x1-7/8"

    2 2 PR LRG NITRILE GLVES ZIP BAG

    6 WATER-JEL BURN DRESSING 2 X 6

    6 WATER-JEL BURN DRESSING 2 X 2

    2 TRI BNDG NON WOVEN 40"X40"X56"

    1 STING Relief SWAB 10

    1 RED BIO BAGS 2/BX

    Close
  • Eyewash Principal Display Panel
  • Ammonia Principal Display Panel
  • Water Soluble 1st Aid Spray Principal Display Panel
  • Burn Relief Water Soluble Principal Display Panel
  • Triple Principal Display Panel
  • Alcohol Principal Display Panel
  • Miralac Principal Display Panel
  • BZK Principal Display Panel
  • Aypanal Principal Display Panel
  • Hydrocortisone Principal Display Panel
  • Sting Relief Principal Display Panel
  • Pain Stopper Principal Display Panel
  • Sinus Decongestant Principal Display Panel
  • Tetrahydrozoline HCL Principal Display Panel
  • 4248 Kit Label 68600PROAM
  • INGREDIENTS AND APPEARANCE
    4248 FIRST AID KIT 
    4248 first aid kit kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-4248
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-4248-01 1 in 1 KIT; Type 0: Not a Combination Product 10/18/2018
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 2 BOTTLE 236 mL
    Part 2 10 AMPULE 3 mL
    Part 3 1 CAN 85 g
    Part 4 1 CAN 85 g
    Part 5 20 PACKET 10 g
    Part 6 50 POUCH 20 mL
    Part 7 125 PACKET 250 
    Part 8 20 PACKET 28 mL
    Part 9 125 PACKET 250 
    Part 10 30 PACKET 27 g
    Part 11 10 POUCH 4 mL
    Part 12 125 PACKET 250 
    Part 13 50 PACKET 100 
    Part 14 1 BOTTLE, DROPPER 15 mL
    Part 1 of 14
    EYESALINE EMERGENCY EYEWASH 
    purified water liquid
    Product 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:0498-0100-02 118 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 2 of 14
    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 3 of 14
    FIRST AID ANTISEPTIC WATER SOLUBLE 
    benzethonium chloride, benzocaine spray
    Product Information
    Item Code (Source) NDC:0498-0031
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.2 g  in 100 g
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 10 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    ISOBUTANE (UNII: BXR49TP611)  
    BUTANE (UNII: 6LV4FOR43R)  
    PROPANE (UNII: T75W9911L6)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0031-40 85 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 part333E 09/19/2018
    Part 4 of 14
    BURN WATER SOLUBLE 
    benzocaine, benzethonium chloride, menthol spray
    Product Information
    Item Code (Source) NDC:0498-0021
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.2 g  in 100 g
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 10 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.33 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    ISOBUTANE (UNII: BXR49TP611)  
    BUTANE (UNII: 6LV4FOR43R)  
    PROPANE (UNII: T75W9911L6)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0498-0021-40 85 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 11/12/2018
    Part 5 of 14
    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
    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:0498-0750-36 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 6 of 14
    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 7 of 14
    MIRALAC 
    calcium carbonate tablet
    Product Information
    Item Code (Source) NDC:0498-0303
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE 420 mg
    Inactive Ingredients
    Ingredient Name Strength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SORBITOL (UNII: 506T60A25R)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    Color white Score 2 pieces
    Shape ROUND Size 11mm
    Flavor MINT Imprint Code FR8
    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 final part331 02/22/2012
    Part 8 of 14
    ANTISEPTIC TOWELETTE 
    benzalkonium chloride liquid
    Product 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 12/22/2017
    Part 9 of 14
    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
    Part 10 of 14
    HYDROCORTISONE 
    anti-itch cream ointment
    Product 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
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    WATER (UNII: 059QF0KO0R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    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
    Part 11 of 14
    STING RELIEF PAD 
    ethyl alcohol, lidocaine swab
    Product 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
    MENTHOL (UNII: L7T10EIP3A)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    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 12 of 14
    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
    CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE 32.4 mg
    SALICYLAMIDE (UNII: EM8BM710ZC) (SALICYLAMIDE - UNII:EM8BM710ZC) SALICYLAMIDE 152 mg
    ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 162 mg
    Inactive Ingredients
    Ingredient Name Strength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    POVIDONE K30 (UNII: U725QWY32X)  
    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 13 of 14
    SINUS DECONGESTANT 
    phenylephrine tablet
    Product Information
    Item Code (Source) NDC:0498-3331
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg
    Inactive Ingredients
    Ingredient Name Strength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SHELLAC (UNII: 46N107B71O)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    D&C RED NO. 27 (UNII: 2LRS185U6K)  
    CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    TALC (UNII: 7SEV7J4R1U)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    Product Characteristics
    Color red Score no score
    Shape OVAL Size 11mm
    Flavor Imprint Code FR4
    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 final part341 09/18/2018
    Part 14 of 14
    EYE DROPS 
    tetrahydrozoline hydrochloride solution/ drops
    Product Information
    Item Code (Source) NDC:0498-0161
    Route of Administration OPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE 0.05 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    BORIC ACID (UNII: R57ZHV85D4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 15 mL in 1 BOTTLE, DROPPER; 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 07/04/2018
    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(0498-4248)
    Establishment
    Name Address ID/FEI Business Operations
    Ultra Seal Corporation 085752004 manufacture(0498-2422, 0498-2001, 0498-0303, 0498-3331)
    Establishment
    Name Address ID/FEI Business Operations
    Dixon Investments 115315822 manufacture(0498-0031, 0498-0021)
    Establishment
    Name Address ID/FEI Business Operations
    Water-Jel Technologies 155522589 manufacture(0498-0750, 0498-0800)
    Establishment
    Name Address ID/FEI Business Operations
    Honeywell Safety Products USA, Inc. 167518617 manufacture(0498-0100)
    Establishment
    Name Address ID/FEI Business Operations
    KC PharmaceuticLS, INC. 174450460 manufacture(0498-0161)
    Establishment
    Name Address ID/FEI Business Operations
    Changzhou Maokang Medical 421317073 manufacture(0498-0143, 0498-0501)
    Establishment
    Name Address ID/FEI Business Operations
    Safetec of America Inc 874965262 manufacture(0498-0733)
    Close