Label: CARE SCIENCE OSHA FIRST AID- ethyl alcohol, isopropyl alcohol, bacitracin zinc, neomycin sulfate, polymyxin-b sulfate, diphenhydramine hydrochloride, hydrocortisone, ibuprofen, acetaminophen, water kit

  • NDC Code(s): 47682-167-46, 47682-198-28, 47682-718-99, 47682-803-99, view more
    51142-002-01, 51142-445-21, 61010-1112-1, 61010-2017-0, 61010-5600-1, 61010-5800-1
  • Packager: ASO LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 5, 2024

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

  • CONTENTS – Care Science OSHA First Aid Kit

    Clean68 ITEMS
    39Alcohol Prep Pads 1 3/16 IN X 2 5/16 IN (30 MM X 58 MM)

    12Antiseptic Wipes 4 3/4 IN X 7 3/4 IN (120 MM X 196 MM)

    10Hand Sanitizers 1/32 OZ (0.9 G)

    6Hand Cleansing Wipes 4 3/4 IN X 7 3/4 IN (120 MM X 196 MM)

    1Eye Wash 1 FL OZ (30 ML)

    Treat40 ITEMS

    14Triple Antibiotic Ointments 1/32 OZ (0.9 G)

    10Topical Cooling Gel 1/8 OZ (3.5 G)

    1Acetaminophen (Non-aspirin) 2 Per Packet

    1Diphen Allergy Caplet 1 Per Packet

    10Hydrocortisone Cream 1/32 OZ (0.9 G)

    2Ibuprofen 2 Per Packet

    1Burn Dressing 4 IN X 4 IN (101 MM X 101 MM)

    1Instant Cold Pack, Single Use 4 IN X 5 IN (101 MM X 125 MM)

    Protect226 ITEMS

    70Sheer Bandages 3/4 IN X 3 IN (19 MM X 76 MM)

    40Sheer Bandages 1 IN X 3 IN (25 MM X 76 MM)

    8Gauze Pads 2 IN x 2 IN (50 MM x 50 MM)

    4Transparent Dressings 2 3/8 IN X 4 IN (60 MM X 101 MM)

    2Eye Cover Pads 2.25 IN x 3.03 IN (57 MM x 77 MM)

    60Sheer Bandages 3/8 IN X 1 1/2 IN (9.5 MM X 38 MM)

    35Butterfly Closures 1 3/4 IN X 3/8 IN (44 MM X 9.5 MM)

    4Gauze Pads 4 IN x 4 IN (101 MM x 101 MM)

    2Trauma Pads 5 in x 9 in (127 MM x 228 MM)

    1Rolled Gauze 4 IN x 2 1/2 YDS (101 MM x 2.2 M)

    Instruments17 ITEMS

    7Wooden Finger Splints

    1CPR Breathing Barrier

    1Triangular Sling 40 IN X 40 IN X 56 IN (101 CM X 101 CM X 142 CM)

    1Metal Tweezers

    4Nitrile Exam Gloves Non-sterile, single use only

    1Paper Tape 1 IN X 5 YDS (25 MM X 4.5 M)

    1Metal Scissors

    1First Aid Guide

    Adhesive Bandages, Burn Dressing, Butterfly Closures, Eye Cover Pad, Gauze Pads, Rolled Gauze, Transparent Dressings, & Trauma Pads are sterile unless wrapper is opened or damaged.
    Gauze Pads and Rolled Gauze are Rayon-polyester blend.

    Kit contents are not made with natural rubber latex.

    Alcohol Prep Pads, Eye Wash, Acetaminophen (Non-Aspirin), Diphen Allergy Caplets, Hydrocortisone Cream, Ibuprofen, & Triple Antibiotic Ointment

    Caution:This product contains non-prescription drug products that have expiration dates. Please check before use. Keep these and all drug products out of the reach of children. Tamper evident sealed packets; do not use any opened or torn packets.


    Adhesive Bandages:
    For use on minor cuts, scrapes, & burns.

    Directions:For optimal results, apply bandage to clean, dry skin. Change the dressing daily, when wet, or more often if needed. Single use.

    Warning:For medical emergencies, seek professional help.

    Butterfly Closures:For use on minor cuts, scrapes, & burns.

    Directions:Remove backing tabs from Butterfly Closure. Apply adhesive sections on either side of the wound. Be sure to center the nonstick area over the wound. Change dressing as directed by your health care professional.

    Warning:For medical emergencies, seek professional help.

    Topical Cooling Gel:For minor burns and scalds

    Directions:Apply gel liberally without rubbing it in. Do not use more than 4 times a day. For children under 2 years consult a physician.

    Warning:For external use only. Keep out of eyes. Keep out of reach of children. Use only as directed. If allergic reaction occurs, discontinue use and consult a physician.

    Caution:Not for serious burns. If the condition for which this product is used persists for more than 7 days, or irritation, redness, swelling or pain increases, or a rash or infection develops, discontinue use and consult a physician. Do not use packet if opened or torn.


    Gauze Pads:
    For cleaning wounds.

    Directions:Gently clean the wound with mild soap and water using the gauze pad and carefully dry the affected area. Discard the used pad.

    Warning:In case of deep puncture wounds or serious burns, consult a physician.

    Nitrile Exam Gloves:Non-sterile single use disposable exam gloves.

    Storage:Protect from freezing. Avoid excessive heat. Keep dry. Gloves should be shielded from direct sunlight, fluorescent lighting, x-rays, moisture and Ozone.

    Disposal:Dispose of gloves and all biologically contaminated matter in an appropriate container.

    Paper Tape: For securing wound covers.

    Directions:Use gauze to gently clean in and around injured area with mild soap and water. Dry injured area and apply medication if necessary. Cover wound with non-stick pad or dressing. Secure the dressing with paper tape to help keep out dirt and contaminants.

    Warning:In case of deep puncture wounds or serious burns, consult a physician.

    Rolled Gauze:For securing wound covers.

    Directions:Use gauze to gently clean in and around injured area with mild soap and water. Dry injured area and apply medication if necessary. Cover wound with a non-stick pad or dressing. Secure the dressing in place by loosely wrapping the area with rolled gauze over the top of the dressing. Secure the end of the rolled gauze with tape as needed, being careful not to restrict circulation by wrapping or taping too tightly.

    Warning:In case of deep puncture wounds or serious burns, consult a physician.

    Trauma Pads:For providing extra cushioning and absorption on wound dressings.

    Directions:Carefully cover the wound with a primary, non-stick pad. Place the sterile trauma pad over it for extra absorbency protection. Pad should have the blue line facing up.

    Warning:In case of deep puncture wounds or serious burns, consult a physician.

    Transparent Dressings:Ideal for minor abrasions, cuts, burns, blisters, scrapes, & post-surgical incisions.

    Directions:Gently clean the wound using a gauze pad with mild soap and water. Carefully dry the affected area and apply medication if needed. Cover the wound with the Transparent Dressing. Do not use as a primary dressing on moderately to heavily draining wounds. Do not stretch while applying.

    Warning:For any change in wound condition, signs of infection or if you have serious burns or a deep puncture wound seek immediate professional medical attention.

    Made in USA with globally sourced materials:Antiseptic Wipes, Butterfly Closures, First Aid Guide, Hand Cleansing Wipes, Hand Sanitizers, Hydrocortisone Cream, Instant Cold Pack, Sheer Adhesive Bandages, Topical Cooling Gel, Triple Antibiotic Ointment, Wooden Finger Splints.

    Made in China:Acetaminophen (Non-Aspirin), Alcohol Prep Pads, Breathing Barrier, Burn Dressing, Carrying Case, Diphen Allergy Caplet, Eye Cover Pads, Gauze Pads, Metal Scissors, Metal Tweezers, Nitrile Gloves, Paper Tape, Rolled Gauze, Transparent Dressing, Trauma Pads, Triangular Sling.


    Made in India:
    Ibuprofen.

    Made in Canada:Eye Wash.

    ANSI/ISEA Z308.1-2015, Class A, Type I or II.This kit meets the ANSI/ISEA Z308.1-2015 standard as sold. It contains first aid products which meet performance specifications detailed in the standard at the

    below required minimum fill. It will continue to be compliant only when maintained with products that

    meet the standard at specified quantities.

    REQUIRED MINIMUM FILL

    16Adhesive Bandages - 1 IN X 3 IN

    1Adhesive Tape - 2 1/2 YDS Total

    10Antibiotic Application - 1/57 OZ

    10Antiseptic - 1/57 OZ

    1Breathing Barrier

    1Burn Dressing (Gel Soaked) - 4 IN X 4 IN

    10Burn Treatment - 1/32 OZ

    1Cold Pack - 4 IN X 5 IN

    2Eye Covering With Means Of Attachment - 2.9 SQ IN

    1Eye/skin Wash - 1 FL OZ Total

    1First Aid Guide

    6Hand Sanitizer - 1/32 OZ

    2 PairMedical Exam Gloves

    1Roller Bandage - 2 IN X 4 YDS

    1Scissors

    2Sterile Pads - 3 IN X 3 IN

    2Trauma Pad - 5 IN X 9 IN

    1Triangular Bandage - 40 IN X 40 IN X 56 IN

    The described kit may be suitable for some businesses. However, the adequacy of the contents for hazards of each work environment should always be evaluated by competent personnel. Kits should be inspected frequently to ensure the completeness and usability of all first aid supplies. Any supply beyond its marked expiration date should be discarded and replaced. For a variety of operations, employers may find that additional first aid supplies and kits are needed.

    PEEL HERE FOR DRUG FACTS & WARNINGS

  • Active ingredient (in each caplet)– Diphen Allergy Caplet

    Diphenhydramine Hydrochloride 25 mg

  • Purpose – Diphen Allergy Caplet

    Antihistamine

  • Uses – Diphen Allergy Caplet

    Temporarily relieves these symptoms due to hay fever or other respiratory allergies

    • runny nose
    • sneezing
    • itching of the nose or throat
    • itchy, watery eyes

    Temporarily relieves these symptoms due to the common cold

    • runny nose
    • sneezing
  • Warnings – Diphen Allergy Caplet

    Do not use – Diphen Allergy Caplet

    • to make a child sleepy
    • with any other product containing diphenhydramine, even one that is used on skin.

    Ask a doctor before use if you have – Diphen Allergy Caplet

    • a breathing problem such as emphysema or chronic bronchitis
    • trouble urinating due to an enlarged prostate gland
    • glaucoma

    Ask a doctor or pharmacist before use if you are – Diphen Allergy Caplet

    • taking sedatives or tranquilizers

    When using this product – Diphen Allergy Caplet

    • marked drowsiness may occur
    • avoid alcoholic drinks
    • alcohol, sedatives and tranquilizers may increase the drowsiness effect
    • use caution when driving a motor vehicle or operating machinery
    • excitability may occur, especially in children

    If pregnant or breast-feeding, – Diphen Allergy Caplet

    ask a health care professional before use.

    Keep out of reach of children. – Diphen Allergy Caplet

    In case of overdose, contact a physician or poison control center right away (1-800-222-1222).

  • Directions – Diphen Allergy Caplet

    • take every 4-6 hours, or as directed by a doctor
    • do not take more than 6 times in 24 hours

    Adults and children: (12 years and over)1 to 2 caplets

    Children under 12 years:do not use

  • Other information – Diphen Allergy Caplet

    • protect from light
    • store at room temperature 68º-77ºF (20º-25ºC)
    • tamper-evident sealed packets
    • do not use any opened or torn packets
  • Inactive Ingredients – Diphen Allergy Caplet

    croscarmellose sodium, D&C red #27 aluminum lake, hypromellose, lactose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, silicon dioxide, titanium dioxide

  • Questions or comments? – Diphen Allergy Caplet

    1-800-634-7680

  • Active ingredients – Antiseptic Wipes

    Ethyl Alcohol 66.5%

  • Purpose – Antiseptic Wipes

    Antiseptic

  • Uses – Antiseptic Wipes

    Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water

  • Warnings – Antiseptic Wipes

    For external use only
    Flammable: keep away from fire or flame

    Do not use – Antiseptic Wipes

    in the eyes. If this happens, rinse thoroughly with water.

    Stop use and ask a doctor – Antiseptic Wipes

    if irritation or redness develop and persist for more than 72 hours

    Keep out of reach of children – Antiseptic Wipes

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

  • Directions – Antiseptic Wipes

    • tear open packet, remove towelette
    • unfold and use as a washcloth
    • supervise children under 6 years of age
  • Inactive ingredients – Antiseptic Wipes

    aloe vera, fragrance, purified water, triethanolamine

  • Active Ingredient (in each gram) – Triple Antibiotic Ointment

    Bacitracin Zinc (400 units Bacitracin)
    Neomycin Sulfate (3.5 mg Neomycin)
    Polymyxin B Sulfate (Polymyxin B 5000 units)

  • Purpose – Triple Antibiotic Ointment

    First Aid Antibiotic
    First Aid Antibiotic
    First Aid Antibiotic

  • Uses – Triple Antibiotic Ointment

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

  • Warnings – Triple Antibiotic Ointment

    For external use only

    Do not use – Triple Antibiotic Ointment

    • internally
    • in eyes
    • over large areas of the body or on puncture wounds, animal bites or serious burns
    • for more than 1 week unless directed by a doctor
    • if you are allergic to any of the ingredients

    Stop use and ask a doctor if – Triple Antibiotic Ointment

    • a rash or allergic reaction develops
    • condition worsens or persists

    Keep out of reach of children – Triple Antibiotic Ointment

    If ingested, contact a Poison Control Center right away.

  • Directions – Triple Antibiotic Ointment

    • clean affected area
    • apply a small amount 1 to 3 times daily
    • may cover with a sterile bandage
  • Inactive ingredients – Triple Antibiotic Ointment

    petrolatum

  • Active Ingredient – Hydrocortisone Cream

    Hydrocortisone 1.0%

  • Purpose – Hydrocortisone Cream

    Anti-itch

  • Uses – Hydrocortisone Cream

    For temporary relief of itching associated with minor skin irritations, inflammation or rashes. Other uses of product should be only under the advice and supervision of a doctor.

  • Warnings – Hydrocortisone Cream

    For external use only

    Do not use – Hydrocortisone Cream

    • in eyes
    • for treatment of diaper rash
    • for feminine itching

    Stop use, ask a doctor – Hydrocortisone Cream

    • if condition worsens or lasts more than 7 days, or clears up and occurs again within a few days
    • with use of other hydrocortisone products

    Keep out of reach of children. – Hydrocortisone Cream

    If ingested, contact a Poison Control Center right away

  • Directions – Hydrocortisone Cream

    • apply to affected area not more than 3 to 4 times daily
    • children under 2: ask a doctor
  • Inactive ingredients – Hydrocortisone Cream

    emulsifying wax, ethanol, methylparaben, mineral oil, paraffin, petrolatum, propylparaben, purified water, white wax

  • Active ingredient – Alcohol Prep Pads

    Isopropyl Alcohol 70%

  • Purpose – Alcohol Prep Pads

    Antiseptic

  • Uses – Alcohol Prep Pads

    • For preparation of the skin prior to an injection
  • Warnings – Alcohol Prep Pads

    For external use only
    Flammable, keep away from fire or flame

    Do not use – Alcohol Prep Pads

    • with electrocautery procedures
    • in the eyes. If contact occurs, flush eyes with water.

    Stop use if – Alcohol Prep Pads

    irritation and redness develop. If condition continues, consult your health care practitioner

    Keep out of reach of children. – Alcohol Prep Pads

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

  • Directions – Alcohol Prep Pads

    • wipe injection area and discard
  • Other information – Alcohol Prep Pads

    • Store at room temperature: 59ºF - 86ºF (15ºC - 30ºC)
  • Inactive ingredient – Alcohol Prep Pads

    purified water

  • Active ingredient – Hand Sanitizer

    Ethyl Alcohol 66.5%

  • Purpose – Hand Sanitizer

    Antiseptic

  • Uses – Hand Sanitizer

    For handwashing to decrease bacteria on skin without soap and water.

  • Warnings – Hand Sanitizer

    For external use only
    Flammable, keep away from fire or flame.

    Keep out of reach of children. – Hand Sanitizer

    Do not use – Hand Sanitizer

    in eyes, if this happens, rinse thoroughly with water.

    Stop use, ask a doctor if – Hand Sanitizer

    irritation develops and persists for 72 hours. If ingested, get medical help or contact a Poison Control Center right away.

  • Directions – Hand Sanitizer

    • wet hands & wrists thoroughly with product and allow to dry without wiping
  • Inactive ingredients – Hand Sanitizer

    aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

  • Active ingredient ( in each tablet) – Ibuprofen

    Ibuprofen 200 mg (NSAID*)
    *nonsteroidal anti-inflammatory drug

  • Purpose – Ibuprofen

    Pain reliever/fever reducer

  • Uses – Ibuprofen

    Temporarily relieves minor aches and pains associated with

    • headache • toothache • backache • menstrual cramps
    • common cold • muscular aches • minor arthritis pain

    Temporarily reduces fever.

  • Warnings – Ibuprofen

    Allergy alert:Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:
    • hives • skin reddening • asthma (wheezing) • facial swelling • rash • shock • blisters
    If an allergic reaction occurs, stop use and seek medical help right away.

    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

    Heart attack or stroke warning:NSAIDS, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

    Do not use – Ibuprofen

    • if you have ever had an allergic reaction to any other pain reliever/fever reducer
    • right before or after heart surgery

    Ask a doctor before use if – Ibuprofen

    • you have problems or serious side effects from taking pain relievers or fever reducers
    • stomach bleeding warning applies to you
    • you have a history of stomach problems such as heartburn
    • you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma or had a stroke
    • you are taking a diuretic

    Ask a doctor or pharmacist before use if you are – Ibuprofen

    • taking aspirin for heart attack or stroke, because ibuprofen may decrease this benefit of aspirin
    • under a doctor’s care for any serious condition
    • taking any other drug

    When using this product – Ibuprofen

    • take with food or milk if stomach upset occurs

    Stop use and ask a doctor if – Ibuprofen

    • you experience any of the following signs of stomach bleeding

    • feel faint • vomit blood
    • have bloody or black stools
    • have stomach pain that does not get better

    • you have symptoms of heart problems or stroke

    • chest pain • trouble breathing
    • weakness in one part or side of body
    • slurred speech • leg swelling

    • pain gets worse or lasts for more than 10 days
    • fever gets worse or lasts for more than 3 days
    • redness or swelling is present in the painful area
    • any new or unexpected symptoms occur

    If pregnancy or breast-feeding, – Ibuprofen

    ask a health professional before use. It is especially important not to use ibuprofen at 20 weeks or later in pregnancy unless specifically directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

    Keep out of reach of children. – Ibuprofen

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions – Ibuprofen

    do not use more than directed
    the smallest effective dose should be used
    • do not take longer than 10 days, unless directed by a doctor (see Warnings)

    Adults and children: (12 years and older)

    Take 1 tablet every 4 to 6 hours while symptoms persist. If pain or fever does not respond to 1 tablet, 2 tablets may be used. Do not exceed 6 tablets in 24 hours, unless directed by a doctor.

    Children under 12 years:

    Ask a doctor

  • Other information – Ibuprofen

    • read all product information before using
    • store at 68-77°F (20-25°C)
    • avoid excessive heat 104°F (above 40°C )
    • tamper evident sealed packets
    • do not use any opened or torn packets
  • Inactive ingredients – Ibuprofen

    carnauba wax*, corn starch, hypromellose*, iron oxide red, lactose*, magnesium stearate*, microcrystalline cellulose*, polydextrose*, polyethylene glycol, polyvinyl alcohol*, povidone (K30)*, silicon dioxide, sodium starch glycolate, stearic acid, talc*, titanium dioxide

    *may contain

  • Questions or comments? – Ibuprofen

    1-800-634-7680

  • Active ingredient ( in each tablet) – Acetaminophen

    Acetaminophen 325 mg

  • Purpose – Acetaminophen

    Pain reliever/fever reducer

  • Uses – Acetaminophen

    temporarily relieves minor aches and pains due to:

    • headache
    • muscular aches
    • minor arthritis pain
    • backache
    • the common cold
    • toothache
    • premenstrual and menstrual cramps

    temporarily reduces fever

  • Warnings – Acetaminophen

    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
    • 3 or more alcoholic drinks every day while using this product

    Allergy alert: – Acetaminophen

    Acetaminophen may cause severe skin reactions. Symptoms may include:

    • skin reddening
    • blisters
    • rash

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

    Do not use – Acetaminophen

    • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
    • if you are allergic to acetaminophen or any of the inactive ingredients in this product

    Ask a doctor before use if you have – Acetaminophen

    • liver disease

    Ask a doctor or pharmacist before use if – Acetaminophen

    • you are taking the blood thinning drug warfarin

    Stop use and ask a doctor if – Acetaminophen

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

    These could be signs of a serious condition

    If pregnant or breast-feeding, – Acetaminophen

    ask a health professional before use.

    Keep out of reach of children. – Acetaminophen

    Overdose warning: – Acetaminophen

    In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

  • Directions – Acetaminophen

    do not use more than directed (see overdose warning)

    Adults and children: (12 years and over)

    • take 2 tablets every 4 to 6 hours while symptoms last
    • do not take more than 10 tablets in 24 hours, unless directed by a doctor
    • do not use for more than 10 days unless directed by a doctor

    Children under 12 years:

    • ask a doctor
  • Other information – Acetaminophen

    • store at room temperature 59°-86°F (15°-30°C)
    • tamper-evident sealed packets
    • do not use any opened or torn packets
  • Inactive Ingredients – Acetaminophen

    corn starch, hypromellose, polyethylene glycol, povidone, pregelatinized starch, sodium starch glycolate, stearic acid, titanium dioxide.

  • Questions or comments? – Acetaminophen

    1-800-634-7680

  • Active ingredient – Eyewash

    Purified water 98.3%

  • Purpose – Eyewash

    Eyewash

  • Use – Eyewash

    For cleansing the eye to help relieve irritation or burning by removing loose foreign material.

  • Warnings – Eyewash

    For external use only

    Do not use – Eyewash

    • if you experience any open wounds in or near the eyes and obtain immediate medical treatment
    • if solution changes color or becomes cloudy

    When using this product – Eyewash

    • to avoid contamination, do not touch tip of container to any surface
    • do not reuse
    • once opened, discard

    Stop use and ask a doctor if you experience – Eyewash

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

    Keep out of reach of children. – Eyewash

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

  • Directions – Eyewash

    Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle.

  • Other information – Eyewash

    • lot number is printed on the bottle
    • store at 20º to 25º C (68º to 77º F)
    • for your protection, this bottle has an imprinted white seal with black printing “TAMPER EVIDENT SEAL”
    • do not use if this seal is missing or broken
    • use before expiration date marked on bottle
  • Inactive ingredients – Eyewash

    boric acid, sodium borate, sodium chloride

  • Questions? – Eyewash

    Call 800-634-7680

  • Principal Display Panel – Care Science OSHA First Aid Kit

    CARE SCIENCE ®

    MEETS OSHA ANSI/ISEA
    Z308.1-2015 Guidelines

    FIRST AID

    OFFICE     HOME     OUTDOOR     SCHOOL

    351 PIECES
    351 PIECES + 1 CARRYING CASE
    See back panel for details

    • Includes first aid essentials for complete wound care + additional supplies
    • Organized shelves for quick access & easy restocking
    • Wall mounts for easy access in any setting


    ASO
    CARE SCIENCE ®
    is an ASO brand
    Distributed by ASO LLC
    Sarasota, Fl 34240
    www.asocorp.com

    image-01-Kit

    Label

  • Principal Display Panel – Diphen Allergy Caplet

    Collect MediBucks See inside flap for more details

    Medique®

    Diphen

    Hay Fever / Allergies

    THIS PACKAGE IS FOR HOUSEHOLDS WITHOUT YOUNG CHILDREN.
    Pull to Open

    Antihistamine• Diphenhydramine HCl 25 mg

    200 Caplets
    (200 x 1)

    Tamper Evident Unit Dose Packets

    Image-02-Dephen

    Label

  • Principal Display Panel – Antiseptic Wipes

    Safetec

    Antiseptic
    Towelette

    For Professional and Hospital Use
    Contents: 1 single-use, premoistened towelette

    Manufactured by SAFETEC OF AMERICA, Inc.
    Buffalo, NY 14215 800-456-7077 www.safetec.com

    image-03

    Label

  • Principal Display Panel – Triple Antibiotic Ointment

    Safetec

    Triple Antibiotic
    Ointment

    0.9 g (1/32 oz.)

    Safetec of America, Inc.
    Buffalo, NY 14215
    800-456-7077

    image-04

    Label

  • Principal Display Panel – Hydrocortisone Cream

    Safetec

    1% Hydrocortisone Cream™
    0.9 g (1/32 oz.)

    Safetec of America, Inc.
    Buffalo, NY 14215
    800-456-7077

    image-05-HC-Cream

    Label

  • Principal Display Panel – Alcohol Prep Pads

    ALCOHOL
    PREP PAD
    1 Pad/Pouch
    Saturated with 70% Isopropyl Alcohol
    For External Use Only

    DO NOT REUSE

    NOT MADE WITH
    NATURAL RUBBER LATEX

    Made in China
    Manufactured for Aso LLC
    Sarasota, Fl 34240 | www.asocorp.com
    DIE 40015

    image-06-AlcoholPads

    Label

  • Principal Display Panel – Hand Sanitizer

    Safetec

    A.B.H.C. ™ MEETS CDC HANDWASHING RECOMMENDATIONS

    Instant
    Hand
    Sanitizer

    0.9 g (1/32 oz.)

    Safetec of America, Inc.
    Buffalo, NY 14215
    800-456-7077

    image-07-Sanitizer

    Label

  • Principal Display Panel – Ibuprofen

    MEDI-FIRST ®

    Ibuprofen 200 mg
    100 tablets (50 x 2)

    Pain Reliever/Fever Reducer
    Aches, Fever • Ibuprofen (NSAID) 200 mg
    Pull to Open

    Compare active ingredient to:
    Advil ®
    Registered Trademark of Pfizer Consumer Healthcare
    THIS PACKAGE IS FOR HOUSEHOLDS
    WITHOUT YOUNG CHILDREN.
    Tamper Evident Unit Dose Packets

    MEDI-FIRST ®
    Reorder #80833
    Manufactured for
    Medique Products
    Fort Myers, FL 33967
    1-800-634-7680
    www.mediqueproducts.com
    image-08-IBU

    Label

  • Principal Display Panel – Acetaminophen (Non-Aspirin)

    Medi-First ®
    Non-Aspirin
    Aches, Fever • Acetaminophen 325 mg

    Compare active ingredient to:
    Tylenol ®
    Registered Trademark of McNeil Consumer products
    Pull to Open

    Pain Reliever/Fever Reducer

    THIS PACKAGE IS FOR HOUSEHOLDS WITHOUT YOUNG CHILDREN.

    Tamper Evident Unit Dose Packets

    500 Tablets
    (250 x 2)

    image-09-APAP

    Label

  • Principal Display Panel – Eye Wash

    MEDI-FIRST ®
    Purified Water, 98.3%
    Ophthalmic Solution
    Eyewash


    NDC 47682-197-11
    Single Use

    Manufactured for
    Medique Products
    17080 Alico Commerce Ct.
    Fort Myers, FL 33967

    Made in Canada
    Reorder #21511
    Sterile Solution

    16 fl oz [473 mL]

    image-10-EyeWash

    Label

  • INGREDIENTS AND APPEARANCE
    CARE SCIENCE OSHA FIRST AID 
    ethyl alcohol, isopropyl alcohol, bacitracin zinc, neomycin sulfate, polymyxin-b sulfate, diphenhydramine hydrochloride, hydrocortisone, ibuprofen, acetaminophen, water kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51142-002
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51142-002-011 in 1 CASE; Type 0: Not a Combination Product07/20/2023
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 PACKET
    Part 212 PACKET 0.0228 L
    Part 314 POUCH 12.6 g
    Part 410 POUCH 9 g
    Part 539 POUCH 13.26 g
    Part 610 POUCH 0.34 L
    Part 72 PACKET
    Part 81 PACKET
    Part 91 BOTTLE, DISPENSING 30 mL
    Part 1 of 9
    MEDIQUE DIPHEN 
    diphenhydramine hydrochloride tablet, film coated
    Product Information
    Item Code (Source)NDC:47682-167
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
    Inactive Ingredients
    Ingredient NameStrength
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    D&C RED NO. 27 (UNII: 2LRS185U6K)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Colorpink (pink) Scoreno score
    ShapeOVAL (OVAL) Size11mm
    FlavorImprint Code 048;D
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-167-461 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01201/01/2012
    Part 2 of 9
    ANTISEPTIC 
    alcohol cloth
    Product Information
    Item Code (Source)NDC:61010-2017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL665 mL  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61010-2017-00.0019 L in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/01/2017
    Part 3 of 9
    TRIPLE ANTIBIOTIC 
    bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment
    Product Information
    Item Code (Source)NDC:61010-5600
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 [USP'U]  in 1 g
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 [USP'U]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61010-5600-10.9 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00408/08/2011
    Part 4 of 9
    HYDROCORTISONE 
    hydrocortisone cream
    Product Information
    Item Code (Source)NDC:61010-5800
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61010-5800-10.9 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/15/2010
    Part 5 of 9
    ALCOHOL PREP PAD 
    alcohol prep pad swab
    Product Information
    Item Code (Source)NDC:51142-445
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (white pad) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51142-445-210.34 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/24/2018
    Part 6 of 9
    INSTANT HAND SANITIZER 
    alcohol gel
    Product Information
    Item Code (Source)NDC:61010-1112
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL665 mL  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    ALOE (UNII: V5VD430YW9)  
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61010-1112-10.034 L in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/15/2010
    Part 7 of 9
    MEDI-FIRST IBUPROFEN 
    ibuprofen tablet, coated
    Product Information
    Item Code (Source)NDC:47682-718
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    POVIDONE K30 (UNII: U725QWY32X)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    TALC (UNII: 7SEV7J4R1U)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    Product Characteristics
    Colorred (Reddish Brown) Scoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code G;2
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-718-992 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07917401/26/2017
    Part 8 of 9
    MEDI-FIRST NON-ASPIRIN 
    acetaminophen tablet, coated
    Product Information
    Item Code (Source)NDC:47682-803
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    Product Characteristics
    Colorwhite (WHITE) Scoreno score
    ShapeROUND (ROUND) Size10mm
    FlavorImprint Code AZ;234
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-803-992 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/30/2008
    Part 9 of 9
    MEDI-FIRST FIRST AID EYE WASH 
    purified water solution
    Product Information
    Item Code (Source)NDC:47682-198
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER983 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BORIC ACID (UNII: R57ZHV85D4)  
    SODIUM BORATE (UNII: 91MBZ8H3QO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-198-2830 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02230510/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/20/2023
    Labeler - ASO LLC (152793493)