OFFICE FIRST AID KIT- first aid kit kit

Office First Aid Kit by

Drug Labeling and Warnings

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

Drug Details [pdf]

HOW SUPPLIED

Office First Aid Kit

25 Person / Contains over 131 pieces

CLEANSE

Antiseptics

50 Alcohol Pads

TREAT

Injury Treatment

1 Instant cold pack

Ointments

2 Antibiotic packets
2 Burn cream packets

PROTECT

Adhesive Bandages

50 Adhesive plastic bandages, 3/4” x 3”

Non-Adhesive Bandages

4 Gauze pads 2" x 2"
6 Gauze pads 3" x 3'
1 Elastic bandage

Tape

1 First aid tape roll, 1/2” x 5 yds

Gloves
10 Medical grade gloves

Other

1 First aid handbook
1 Registration card

Implements

1 Scissors
1 Tweezers, plastic

GENERAL PRECAUTIONS

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

REFERENCES

Foreign item origin: China
Alcohol Pads, Instant cold pack, Adhesive
plastic bandages, Gauze pads, Elastic bandage,
First aid tape roll, Gloves, First aid handbook,
Registration card, Scissors,Tweezers.

PRINCIPAL DISPLAY PANEL

Acme United Corporation
60 Round Hill Road
Fairfield, CT 06824

www.acmeunited.com
Designed in the USA | Made in China
©2010 Acme United Corporation

PhysiciansCare® and Acme are registered
trademarks of Acme United Corporation.

Prep Pad Labeling

Reorder 51019

NDC: 65517-0001-1

Physicians Care

Alcohol Prep Pad

Saturated with 70% Isopropyl Alcohol

For External Use Only

1 Prep Pad

Acme United Corporation, 60 Round Hill Road, Fairfield, CT 06824

Made in China

Drug Facts

Active Ingredients..................... Isopropyl Alcohol 70%

Purpose.................................  Antiseptic Cleanser

Use For preparation of the 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 or 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

25 Person - First Aid Kit Label

Content Card Label

Prep Pad Label

Triple Antibiotic Label

Burn Cream Label

INGREDIENTS AND APPEARANCE

OFFICE FIRST AID KIT 
first aid kit kit

Product Information
Product Type	MEDICAL DEVICE	Item Code (Source)	NDC: 65517-0018

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65517-0018-1	1 in 1 PACKAGE, COMBINATION

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	50 POUCH	20 mL
Part 2	2 PACKET	1.8 g
Part 3	2 PACKET	1.8 g

Part 1 of 3

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 3

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 3

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

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)