READY CARE KIT- first aid kit kit

Ready Care Kit by

Drug Labeling and Warnings

Ready Care Kit by is a Other medication manufactured, distributed, or labeled by Dukal Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

Physicians Care

FIRST AID

25 Person

ReadyCare Kit

Contains over 182 Pieces

Back Label

Physicians Care

CLEANSE

Antiseptics

14    Antiseptic Wipes
16    Alcohol Pads

TREAT

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

PROTECT

16     3/8” x 1 1/2” Bandages
16     1” x 3” Bandages
80     3/4” x 3” Bandages
1      1/2" Tape
1      Triangular Bandage
4      3" x 3" Sterile Gauze Pads
1      Abdominal Compress

Other

Medical Exam Latex Gloves (2 Pair)
1       Tweezers
1       Cold Pack
1       First Aid Guide
10     Finger Splints

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

• For External Use Only
• Flammable, Keep away from fire or flame

Do Not Use

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

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

Ready Care Kit Front Label

Ready Care Kit Back Label

Prep Pad Label

BZK Towelette Label

Triple Antibiotic Label

Burn Cream Label

INGREDIENTS AND APPEARANCE

READY CARE KIT 
first aid kit kit

Product Information
Product Type	MEDICAL DEVICE	Item Code (Source)	NDC: 65517-0020

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65517-0020-1	1 in 1 PACKAGE, COMBINATION

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	16 POUCH	6.4 mL
Part 2	6 PACKET	5.4 g
Part 3	6 PACKET	5.4 g
Part 4	14 POUCH	19.6 mL

Part 1 of 4

DUKAL ALCOHOL PREP PAD 
isopropyl alcohol swab

Product Information
Item Code (Source)	NDC: 65517-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.70 mL  in 1.0 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65517-0001-1	0.4 mL in 1 POUCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2000

Part 2 of 4

WATER-JEL 3-IN1 ANTIBIOTIC 
bacitracin zinc, polymyxin b sulfate and neomycin sulfate ointment

Product Information
Item Code (Source)	NDC: 59898-740
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN ZINC	400 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN SULFATE	3.5 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B SULFATE	5000 [iU]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59898-740-01	0.9 g in 1 PACKET

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333	01/01/2010

Part 3 of 4

FIRST AID BURN 
lidocaine hydrochloride and benzalkonium chloride cream

Product Information
Item Code (Source)	NDC: 59898-902
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59898-902-01	0.9 g in 1 PACKET

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333	01/01/2010

Part 4 of 4

BZK TOWELETTE 
benzalkonium chloride swab

Product Information
Item Code (Source)	NDC: 65517-0004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.00186 mL  in 1.4 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	1.39814 mL  in 1.4 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65517-0004-1	1.4 mL in 1 POUCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2006

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333	05/01/2010

Labeler - Dukal Corporation (791014871)