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

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Care Science OSHA First Aid Kit

CONTENTS – Care Science OSHA First Aid Kit

Clean 68 ITEMS
39 Alcohol Prep Pads 1 3/16 IN X 2 5/16 IN (30 MM X 58 MM)

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

10 Hand Sanitizers 1/32 OZ (0.9 G)

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

1 Eye Wash 1 FL OZ (30 ML)

Treat 40 ITEMS

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

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

1 Acetaminophen (Non-aspirin) 2 Per Packet

1 Diphen Allergy Caplet 1 Per Packet

10 Hydrocortisone Cream 1/32 OZ (0.9 G)

2 Ibuprofen 2 Per Packet

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

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

Protect 226 ITEMS

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

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

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

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

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

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

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

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

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

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

Instruments 17 ITEMS

7 Wooden Finger Splints

1 CPR Breathing Barrier

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

1 Metal Tweezers

4 Nitrile Exam Gloves Non-sterile, single use only

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

1 Metal Scissors

1 First 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

16 Adhesive Bandages - 1 IN X 3 IN

1 Adhesive Tape - 2 1/2 YDS Total

10 Antibiotic Application - 1/57 OZ

10 Antiseptic - 1/57 OZ

1 Breathing Barrier

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

10 Burn Treatment - 1/32 OZ

1 Cold Pack - 4 IN X 5 IN

2 Eye Covering With Means Of Attachment - 2.9 SQ IN

1 Eye/skin Wash - 1 FL OZ Total

1 First Aid Guide

6 Hand Sanitizer - 1/32 OZ

2 Pair Medical Exam Gloves

1 Roller Bandage - 2 IN X 4 YDS

1 Scissors

2 Sterile Pads - 3 IN X 3 IN

2 Trauma Pad - 5 IN X 9 IN

1 Triangular 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

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)

Revised: 2/2024
Document Id: 1cbace4d-fd0a-41d1-aa71-907d43620bf8
Set id: 1cbace4d-fd0a-41d1-aa71-907d43620bf8
Version: 1
Effective Time: 20240202
 
ASO LLC