READY CARE XL KIT - first aid kit 
Dukal Corporation

----------

Front Label

Physicians Care

FIRST AID

50 Person

ReadyCare XL Kit

Contains over 355 Pieces


Back Label

Physicians Care

CLEANSE

20    Antiseptic Wipes
20    Alcohol Pads

TREAT

 6     Antibiotic Ointment Packets
 6     Burn Ointment Packets
10    3" Cotton Tip Applicators

PROTECT

3       Knuckle Bandages
3       Fingertip Bandages
35     3/8” x 1 1/2” Bandages
16     1” x 3” Bandages
200   3/4” x 3” Bandages
1      1/2" Tape
1      Triangular Bandage
4      3" x 3" Sterile Gauze Pads
1      Abdominal Compress

Medicine

3     Acetaminophen Packets (packet of 2)
3     Aspirin Packets (packets of 2)
3     Antacid Packets (packets of 2)

Other

Gloves (2 Pair)
1       Cold Pack
1       First Aid Guide
10     Finger Splints
5       Disposable Thermometers
1       Tweezer


Acme United Corporation
60 Round Hill Road
Fairfield CT 06824

www.acmeunited.com

Designed in the USA | Made in China

CAUTION: This product may contain natural
rubber latex which may cause allergic reactions.
This kit contains products that have expiration dates. Please check before use.

BZK Towelette Labeling

Reorder 855

NDC 65517-0004-1

Dukal

BZK TOWELETTE

Contains Benzalkonium Chloride

For External Use Only

Helps Prevent Infection

1 / Pouch

DUKAL CORPORATION

(631) 656-3800

Ronkonkoma, NY 11779 www.dukal.com

Made in China


Drug Facts

Active Ingredients....................Benzalkonium Chloride 0.133% w/v

Purpose................................. First Aid Antiseptic

USE: Antiseptic Cleansing of face, hands and
body without soap and water. Airs dries in seconds

DO NOT USE: in the eyes or apply over large
areas of the body.

STOP USE: If irritation, redness or other symptoms
develop. Consult a doctor if the conditions persists
or gets worse.

CAUTION: Keep out of reach of children. If
swallowed get medical help or contact a Poison
Control Center right away.

DIRECTIONS: Tear open packet, unfold and use
as a washcloth.

INACTIVE INGREDIENTS: Distilled Water


Prep Pad Labeling

Reorder 852

Dukal Corporation

NDC 65517-0001-1

NPN 80003156

ALCOHOL PREP PAD

Saturated with 70% Isopropyl Alcohol

For External Use Only

1 / Pouch

Dukal Corporation

Ronkonkoma, NY 11779

631-656-3800

www.dukal.com

Made in China


Drug Facts

Active Ingredients

Isopropyl Alcohol 70%

Purpose

Antiseptic Cleanser

Use

For Preparation of Skin prior to an injection

Warnings

Do Not Use

Stop Use

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

Keep out of reach of children

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

Directions

Wipe injection site vigorously and discard.

Other Information

Store at Room Temperature 15 - 30 C (59 - 86 F)

Inactive Ingredient

purified water

Triple Antibiotic Labeling

WaterJel

Triple Antibiotic

First Aid Ointment

To Help Prevent Infection

Each Gram contains

Bacitracin Zinc 400 units

Neomycin Sulphate 5 mg

(equivalent to 3.5 mg Neomycin base)

Polymyxin B Sulfate 5000 units

Water-Jel Technologies

Carlstadt, NJ 07072

Drug Facts

Uses to help prevent infection in

minor cuts, scrapes, burns

Warnings

For external use only

Do not use

in the eyes or apply over large areas of the body

If you are allergic to any of the ingredients

longer than 1 week unless directed by a doctor

Stop use and ask a doctor if

the condition persists or gets worse

a rash or other allergic reaction develops

Keep out of reach of children

if ingested contact Poison Control Center right away

Directions

clean affected area apply a small amount of 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

First Aid Burn Cream Labeling

WaterJel

First Aid Burn Cream

Antiseptic Pain Relief with Aloe

Active Ingredients:

Benzalkonium Chloride 0.13%

Lidocaine HCL 0.5%

Water-Jel Technologies

Carlstadt, NJ 07072

Drug Facts

Purpose

First Aid Antiseptic, External analgesic

Uses

first aid to help prevent infection and for temporary

relief of pain an itching associated with minor cuts,

scrapes, burns

Warnings

For external use only

Do not use

in the eyes

in large quantities over raw or blistered areas or on

deep puncture wounds, animal bites, or serious burns

Keep out of reach of children

if ingested contact Poison Control Center right away

Directions

clean affected area apply a small amount not more

than 3 times daily may be covered with a sterile bandage

Other Information

Store at room temperature

APAP Labeling

Drug Facts
Active Ingredients (In each tablet)...............Purposes
Acetaminophen 325 mg.............................Pain Reliever/Fever Reducer
Uses:
For the temporary relief of minor aches and pains associated with:
• headache • muscular aches • minor arthritis pain
• common cold • toothache • menstrual cramps
For the reduction of fever.
Warnings:
Alcohol Warning: If you consume 3 or more alcoholic drinks every day,
ask your doctor whether you should take acetaminophen or other pain
relievers/fever reducers. Acetaminophen may cause liver damage.
Do not use:
• with any other product containing acetaminophen
• for more than 10 days for pain unless directed by a doctor
• for more than 3 days for fever unless directed by a doctor
Stop Using and Ask a Doctor If:
• symptoms do not improve
• new symptoms occur
• pain or fever persists or gets worse
• redness or swelling is present
Do not exceed recommended dosage. Keep this and all drugs out of the reach of children.
In case of accidental overdose, contact a physician or Poison Control Center immediately.
Prompt medical attention is critical for adults as well as for children even if you do not notice
any signs or symptoms.
If pregnant or breast feeding, ask a health professional before use.
Directions:
Do not use more than directed
Adults and children: (12 years and older)
Take 2 tablets every 4 to 6 hours as needed. Do not take more than 12 tablets in 24 hours,
or as directed by a doctor.
Children under 12 years:
Do not give to children under 12 years of age.
Other Information:
• Store at room temperature
• Tamper-Evident Sealed Packets
• Do Not Use any Opened or Torn Packets
Inactive Ingredients:
Corn starch*, croscarmellose sodium, crospovidone, hypromellose, microcrystalline cellulose,
mineral oil, opadry clear, pharmaceutical glaze, polyethylene glycol, povidone*, pregelatinized
starch*, sodium carboxymethylcellulose, sodium starch glycolate, stearic acid*, talc*, titanium dioxide.
*may contain
Questions or comments? 1-800-634-7680

Alcalak Labeling

Drug Facts
Active Ingredients (In each tablet)....................Purposes
Calcium Carbonate 420 mg ..............................Antacid
Uses:
For the relief of the following symptoms associated with:
• acid indigestion • sour stomach • heartburn • upset stomach
Warnings:
Ask a doctor or health professional before use if you have:
• been taking a prescription drug. Antacids may interact with certain prescription drugs.
• kidney stones
• a calcium-restricted diet
Stop using this product and ask a doctor if:
• symptoms last more than 2 weeks
Do not exceed recommended dosage.
Keep this and all drugs out of the reach of children. If you are pregnant or breast feeding,
ask a health professional before use.
Directions:
• Do not use more than directed
Adults and children: (12 years and older)   
Take 2 tablets every 2 or 3 hours as symptoms occur or as directed by a physician. Do not
take more than 19 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 physician.
Children under 12 years:   
Do not give to children under 12 years of age.
Other Information:
• Phenylketonurics: Contains Phenylalanine 1.5 mg per tablet
• Each tablet contains 168 mg of elemental calcium
• Store at room temperature in a dry place
• Tamper-Evident Sealed Packets
• Do not Use any Opened or Torn Packets
Inactive Ingredients:
aspartame*, carageenan*, croscarmellose sodium*, glycine*, magnesium stearate, mint flavor*,
silica*, sorbitol, spearmint flavor*, stearic acid*, stevix*, xylitol*  
*may contain
Questions or comments? 1-800-634-7680

Aspirin Labeling

Drug Facts
Active Ingredients (In each tablet)..................Purposes
Aspirin 325mg (NSAID*) ...............................Pain Reliever / Fever Reducer
*nonsteroidal anti-inflammatory drug
Uses:
Temporarily relieves minor aches and pains due:
• headache • muscular aches • minor arthritis pain • backache
• common cold • toothache • menstrual cramps
Temporarily reduces fever.
Warnings:
Reye's Syndrome: Children and teenagers should not use this medicine for chicken pox,
or flu symptoms before a doctor is consulted about Reye's Syndrome, a rare but serious
illness reported to be associated with aspirin.
Allergy Alert: Aspirin may cause a severe allergic reaction which may include:
• hives • skin reddening • facial swelling • rash • asthma (wheezing) • blisters • shock
If an allergic reaction occurs, stop use and seek medical help right away.
Stomach Bleeding Warning: This product contains a nonsteroidal anti-inflammatory
drug (NSAID), which may cause 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 an NSAID (aspirin, ibuprofen, naproxen, or others)
• have 3 or more alcohol drinks every day while using this product
• take more or for a longer time than directed
Do not use:
• 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 you have:
• problems or serious side effects from taking pain relievers or fever reducers
• stomach problems that last or come back, such as heartburn, upset stomach, or
stomach pain • ulcers • bleeding problems • high blood pressure
• heart or kidney disease • taken a diuretic • reached age 60 or older
Ask a Doctor or Pharmacist before use if you are:
• taking any other drug containing and NSAID (prescription or nonprescription)
• taking a blood thinning (anticoagulant) or steroid drug
• under a doctor’s care for any serious condition • taking any other drug
When using this product:
• take with food or milk if stomach upset occurs
• long term continuous use may increase the risk of heart attack or stroke
Stop Using and Ask a Doctor If:
• you feel faint, vomit blood, or have bloody or black stools. These are signs of
stomach bleeding. • pain gets worse or lasts more than 10 days
• fever gets worse or lasts more than 3 days • you have difficulty swallowing
• it feels like the pill is stuck in your throat • you develop heartburn
• stomach pain or upset gets worse or lasts
• redness or swelling is present in the painful area • any new symptoms appear
If pregnant or breast-feeding, ask a health 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 delivery.
Keep out of reach of children. In case of overdose, get medical help or contact a
Poison Control Center right away.
Directions:
• Do not take more than directed.
• The smallest effective dose should be used.
• Do not take longer than 10 days, unless directed by a doctor (see Warnings)
• Drink a full glass of water with each dose.
Adults and children: (12 years and older)  
Take 1 or 2 tablets with water every 4 hours as needed. Do not take more than 12 tablets
in 24 hours, or as directed by a doctor.
Children under 12 years:  
Do not give to children under 12 years of age.
Other Information:
• Read all product information before using
• Store at room temperature
• Avoid excessive heat and humidity
• Tamper evident sealed packets
• Do not use any opened or torn packets
Inactive Ingredients:
Corn starch, croscarmellose sodium*, hypromellose*, microcrystalline cellulose*, mineral oil*,
polyethylene glycol, propylene glycol, silicon dioxide, starch, stearic acid, talc, titanium dioxide*.
*may contain
Questions or comments? 1-800-634-7680

Ready Care XL Kit Label

Front Label

Ready Care XL Kit Back Label

Back Label

Prep Pad Labeling

Prep Pad Label

Antiseptic Towelette Label

BZK Label

Antacid Label

Antacid Label

Acetaminophen Label

APAP Label

Aspirin Label

Aspirin Label

Triple Antibiotic Label

Antibiotic Label

Burn Cream Label

Burn Cream Label

READY CARE XL KIT 
first aid kit kit
Product Information
Product TypeMEDICAL DEVICEItem Code (Source)NDC:65517-0021
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65517-0021-11 in 1 PACKAGE, COMBINATION
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 120 POUCH 8.0 mL
Part 26 PACKET 5.4 g
Part 36 PACKET 5.4 g
Part 420 POUCH 28.0 mL
Part 53 PACKET
Part 63 PACKET
Part 73 PACKET
Part 1 of 7
DUKAL ALCOHOL PREP PAD 
isopropyl alcohol swab
Product Information
Item Code (Source)NDC:65517-0001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.70 mL  in 1.0 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65517-0001-10.4 mL in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2000
Part 2 of 7
WATER-JEL 3-IN1 ANTIBIOTIC 
bacitracin zinc, polymyxin b sulfate and neomycin sulfate ointment
Product Information
Item Code (Source)NDC:59898-740
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC400 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE3.5 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B SULFATE5000 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59898-740-010.9 g in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33301/01/2010
Part 3 of 7
FIRST AID BURN 
lidocaine hydrochloride and benzalkonium chloride cream
Product Information
Item Code (Source)NDC:59898-902
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM (UNII: 7FLD91C86K)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
TROLAMINE (UNII: 9O3K93S3TK)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59898-902-010.9 g in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33301/01/2010
Part 4 of 7
BZK TOWELETTE 
benzalkonium chloride swab
Product Information
Item Code (Source)NDC:65517-0004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.00186 mL  in 1.4 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R) 1.39814 mL  in 1.4 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65517-0004-11.4 mL in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2006
Part 5 of 7
MEDIQUE APAP 
acetaminophen tablet, film coated
Product Information
Item Code (Source)NDC:47682-145
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSE (UNII: 3NXW29V3WO)  
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (ROUND) Size10mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-145-992 in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34312/30/2008
Part 6 of 7
MEDIQUE ASPIRIN  
aspirin tablet, film coated
Product Information
Item Code (Source)NDC:47682-116
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN325 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSE (UNII: 3NXW29V3WO)  
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STARCH, CORN (UNII: O8232NY3SJ)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (ROUND) Size10mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-116-992 in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34312/30/2008
Part 7 of 7
MEDIQUE ALCALAK 
calcium carbonate tablet, chewable
Product Information
Item Code (Source)NDC:47682-088
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Calcium Carbonate (UNII: H0G9379FGK) (Calcium - UNII:SY7Q814VUP) Calcium Carbonate420 mg
Inactive Ingredients
Ingredient NameStrength
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
STARCH, CORN (UNII: O8232NY3SJ)  
SUCROSE (UNII: C151H8M554)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (ROUND) Size12mm
FlavorMINT (MINT) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-088-992 in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33112/30/2008
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33305/01/2010
Labeler - Dukal Corporation (791014871)

Revised: 11/2010
Document Id: 8e420537-54ba-478b-a5a4-1042a828c581
Set id: 817e2a80-6d90-42ea-9e85-8daa170f231c
Version: 4
Effective Time: 20101103
 
Dukal Corporation