ACME FIRST AID CONTAINS 404 PIECES- benzalkonium chloride, lidocaine, water, isopropyl alcohol, aspirin, benzocaine, alcohol, bacitracin zinc, neomycin sulfate, polymyxin b sulfate kit

ACME FIRST AID Contains 404 PIECES by

Drug Labeling and Warnings

ACME FIRST AID Contains 404 PIECES by is a Otc medication manufactured, distributed, or labeled by Acme United Corp., GFA Production ( Xiamen) Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENTS:

Benzalkonium Chloride 0.13%
Lidocaine HCL 0.5%

PURPOSE

Purpose: First aid antiseptic, external analgesic

Uses: First aid to help prevent infection and for the temporary relief of pain and itching associated with:

Minor Cuts

Scrapes

Burns

WARNINGS

Warnings:

For external  use only

DO NOT USE

Do not use: In eyes, in large quantities, over raw blistered areas, or on deep puncture wounds, animal bites or serious burns, for more than one week

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of Children.

If ingested, contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions: Clean affected area, Apply small amount not more than 3 times daily.

May be covered with a sterile bandage.

STORAGE AND HANDLING

Other Information:

Store at room temperature

PRINCIPAL DISPLAY PANEL

Genuine First Aid Burn Cream

Antiseptic Pain Relief With Aloe

Net Wt 0.9g (1/32 oz)

Manufactured in CHINA for

Genuine First Aid.

PRINCIPAL DISPLAY PANEL

ACTIVE INGREDIENT

Active Ingredient:                                            Purpose

Benzalkonium Chloride 0.40%..........    First Aid Antiseptic

PURPOSE

Use: For Professional and Hospital use.  Helps prevent infection.  Antiseptic cleansing of face, hands and body without soap and water.

WARNINGS

Warning:    For external use only.

KEEP OUT OF REACH OF CHILDREN

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

STOP USE

Stop use if unusual redness, swelling or other symptoms occur. Consult a physician immediately.

DO NOT USE

Do not use in the eyes or over large areas of the body.

WHEN USING

Directions: Tear open packet, unfold towelette and use to cleanse desired skin area.  Discard towelette appropriately after single use.

INACTIVE INGREDIENT

Inactive Ingredient:    Purified water

DESCRIPTION

LOT/EXP:                                    Made in CHINA

20130301

PRINCIPAL DISPLAY PANEL

Antiseptic Towelette

Genuine First Aid LLC, Clearwater FL 33755

www.GenuineFirstAid.com

1/pouch

GENUINE FIRST AID

PRINCIPAL DISPLAY PANEL

ACTIVE INGREDIENT

Active Ingredient: .........Bacitracin Zinc 400 units

Neomycin Sulfate 5mg ( equivalent to 3.5 mg Neomycin base)

Polymyxin B Sulfate 5000 units

PURPOSE

Uses:  To help prevent infection in:
minor cuts;  scrapes;  burns

WARNINGS

Warnings:

For external use only.

DO NOT USE

Do not use:  in eyes;  over large areas of the body;

If allergic to any of the ingredients;  for more than one week unless directed by a physician.

STOP USE

Stop use and consult a doctor:

if the condition persists or gets worse;  a rash or other allergic reaction develops

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If ingested, contact a Poison

Control Center right away.

WHEN USING

Directions: clean affected area;  apply small amount of this 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

STORAGE AND HANDLING

Other information:

Store at room temperature.

PRINCIPAL DISPLAY PANEL

Genuine Triple Antibiotic

First Aid Ointment

To Help Prevent Infection

Each Gram Contains:

Bacitracin Zinc 400 units

Neomycin Sulfate 5 mg

(equivalent to 3.5 mg

Neomycin base)

 Polymyxin B Sulfate 5000 units

Net Wt. 0.5g ; (1/64 oz)

Manufactured in CHINA for

GENUINE FIRST AID.

PRINCIPAL DISPLAY PANEL

ACTIVE INGREDIENT

Active Ingredient:

Purified Water USP...q.s.

INACTIVE INGREDIENT

Inactive Ingredients:

Sodium Chloride USP                                          44mg

Monobasic Sodium Phosphate USP                18mg
Sodium Phosphate Dibasic USP                       111mg  

Edetate Disodium USP                                       10mg

Benzalkonium Chloride                                      0.5mg
NF (as preservative)

STORAGE AND HANDLING

Store in a cool place. For irrigation only.

Discard unused portion of the solution.

Not for injection.

WARNINGS

Warning:

If you experience eye pain, changes in vision, continued redness or irritation of the eye,

or if the condition worsens or persists for more than 72 hours, discontinue use and consult a doctor.

Do not use if solution changes color or becomes cloudy.

DOSAGE & ADMINISTRATION

Directions

Remove contacts before using.

Twist top to remove.

Flush the affected area as needed. Control

Rate of flow by pressure on the bottle. Do not touch

tip of the container to any surface. Do not reuse.

If necessary continue flushing with emergency eyewash or shower.

Discard bottle after use.

PURPOSE

Uses:

For flushing or irrigating the eyes to

remove loose foreign material, air pollutants,

or chlorinated water.

DESCRIPTION

Code No.: GUJ/DRUG/G/1080

Batch No.:

Mfg Date:

Exp: Date:

PRINCIPAL DISPLAY PANEL

10ml

Sterile Isotonic Buffered Genuine

 Eyewash

For single use only

PRINCIPAL DISPLAY PANEL

ACTIVE INGREDIENT

Active Ingredient:                                        Purpose

Isopropyl Alcohol, 70% v/v...............        Antiseptic

PURPOSE

Use:    For preparation of skin before injection.

WARNINGS

Warnings:    For external use only.   

STORAGE AND HANDLING

Flammable - keep away from fire or flame

Store at room temperature 15-30 degree Celsius (59-86 degree Fahrenheit)

DO NOT USE

Do not use: with electrocautery, in the eyes.

STOP USE

Stop use if irritation and redness develop. If condition persists for more than 72 hours, consult your doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.  If swallowed,

get medical help or contact a Poison Control

Center right away.

WHEN USING

Wipe Injection site vigorously and discard.

INACTIVE INGREDIENT

Inactive Ingredient:    Purified water.

DESCRIPTION

LOT/EXP:                Made in CHINA

20140301

PRINCIPAL DISPLAY PANEL

Alcohol Cleansing  Pad
Genuine First Aid LLC, Clearwater FL 33755

www.GenuineFirstAid.com

1/pouch

GENUINE FIRST AID

PRINCIPAL DISPLAY PANEL

ACTIVE INGREDIENT

Active Ingredient:                                    Purpose:

Benzocaine, 6% w/v..................    Topical Anesthetic

SD alcohol, 60% w/v..................    Antiseptic

PURPOSE

Use: For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

WARNINGS

Warnings: For external use only.

Avoid contact with eyes.  If this happens, rinse thoroughly with water.

KEEP OUT OF REACH OF CHILDREN

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

STORAGE AND HANDLING

Flammable - keep away from fire or flame.

DO NOT USE

Do not use: In eyes, on broken skin, deep puncture wounds.  If unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately.

DESCRIPTION

Made in CHINA

LOT/EXP:

PRINCIPAL DISPLAY PANEL

Insect Sting Relief Pad

Genuine First Aid LLC, Clearwater FL 33755
                        www.GenuineFirstAid.com

1/pouch

GENUINE FIRST AID

PRINCIPAL DISPLAY PANEL

ACTIVE INGREDIENT

Active ingredient (in each tablet)                           Purpose

Aspirin 81 mg (NSAID*). . . . . . . . . . . . . Analgesic/Antipyretic

*nonsteroidal anti-inflammatory drug

PURPOSE

Uses

temporary relief of minor aches, pains and headaches

to reduce fever associated with colds, sore throats, teething

WARNINGS

Warnings

Reye's syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of reye's syndrome, a rare but serious illness.
Stomach bleeding warning:  This product contains a non-steroidal anti-inflammatory drug (NSAID), which may cause stomach bleeding.  The chance is higher if the user; has had stomach ulcers or bleeding problems takes a blood thinning (anticoagulant) or steroid drug takes other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others) takes more or for a longer time than directed is age 60 or older has 3 or more alcoholic drinks every while using this product.

DO NOT USE

Do not use

if you are allergic to aspirin or any other pain relievers/fever reducers

for more than 10 days for pain unless directed by a doctor

for more than 3 days for fever unless directed by a doctor

for at least 7 days after a tonsillectomy or oral surgery

ASK DOCTOR

Ask a doctor before use if you have;

asthma

stomach problems (such as heartburn, upset stomach, or stomach pain) that persist or recur, ulcers or bleeding problems

a child experiencing arthritis pain

if you are;

allergic to aspirin

taking prescription drug for anticoagulation (thinning of blood), diabetes, gout or arthritis

STOP USE

Stop use and ask a doctor if;

an allergic reaction occurs, Seek medical help right away

pain or fever persists

new or unexpected symptoms occur

redness or swelling is present

ringing in ears or loss of hearing occurs

PREGNANCY OR BREAST FEEDING

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 unborn child or complications during delivery.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION

Directions  Do not use more than directed

Adults and Children (12 years and older): Chew 4 to 8 tablets with water every 4 hours,  Do not exceed 48 tablets in 24 hours unless directed by a doctor.

Children Under 12 years: Consult a doctor.

STORAGE AND HANDLING

Store at room temperature

tamper evident sealed packets

do not use any opened or torn packets

INACTIVE INGREDIENT

Inactive ingredients        flavor, FD and C yellow No. 6, saccharin, sodium, silicon dioxide, starch, stearic acid, sucrose

DESCRIPTION

MADE IN USA

Distributed by GENUINE FIRST AID

600 Cleveland Str Suite 400, Clearwater, FL 33755

PRINCIPAL DISPLAY PANEL

 2 Tablets

GENUINE FIRST AID.

Chewable Aspirin 81mg

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PhysiciansCARE

FIRST AID
all purpose kit
with 6 First Aid Pockets

1 Small Cuts and Burns

2 Medium Cuts and Scratches

3 Severe Bleeding and Burns

4 CPR

5 Protection

6 Instruments

New
REFILL PACKS AVAILABLE FOR EACH POCKET

HOME        PLAY    AUTO     OFFICE    WORK  

CONTAINS 1000 PIECES

Soft-Sided Storage Case

With Pockets that are Organized for Quick and Easy Emergency Access

CARRYING CASE
1 Soft-sided Bag
1 Inside Plastic Pockets

SMALL CUTS AND BURNS Pocket One
95 Adhesive Plastic Bandages 3/4"x3"
95 Junior Plastic Bandages 3/8"x1-1/2"
45 Adhesive Plastic Bandages 1"x3"
4 Knuckle Fabric Bandages
56 Adhesive Spot Bandages 7/8"x7/8"
4 Fingertip Fabric Bandages
3 Elbow/Knee Adhesive Bandage
1 Burn Cream
9 Antiseptic Towelettes
2 Triple Antibiotic Ointment
5 Sterile Gauze Pads 2''x2''
20 Cotton Tipped Applicatiors

MEDIUM CUTS AND SCRATCHES Pocket Two
12 Antiseptic Towelettes
5 Sterile Gauze Pad 2"X2"
2 Sterile Gauze Pad 3"x3"
2 Sterile Gauze Pad 4"x4"
1 Roll Gauze Bandages 2"
1 Sterile Eye Pads
1 Sterile Eye Wash
5 Butterfly Wound Closures

SEVERE BLEEDING AND BURNS Pocket Three
1 First Aid Tape Roll 1/2"
1 Combine Pad 5"x9"
1 Combine Pad 8"x10"
1 Roll Gauze Bandage 3"

CPR Pocket Four
1 CPR Breathing Barrier

PROTECTION Pocket Five
2 Medical Grade  Gloves
1 Instant Cold Compress
6 Alcohol Cleansing Pads
2 Insect Sting Relief Pads
1 Emergency Blanket 38"X 60"
4 Chewable Aspirin Tablets
1 Triangular Bandage 42"x42"x59"

INSTRUMENTS Pocket Six
1 Emergency First Aid Guide
1 Plastic Tweezers
1 Scissors
6 Assorted Safety Pins
2 Wooden Finger Splints

CAUTION: This kit contains products that have expiration dates. Please check before using.

Acme United Corporation
60 Round Hill Road
Fairfield, CT 06824
www.acmeunited.com
Designed in USA / Made in India
2009 Acme United Corporation
PhysiciansCare and are Registered Trademrks
of Acme United Corporation

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACME FIRST AID CONTAINS 404 PIECES 
benzalkonium chloride, lidocaine, water, isopropyl alcohol, aspirin, benzocaine, alcohol, bacitracin zinc, neomycin sulfate, polymyxin b sulfate kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-1806

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0924-1806-01	1 in 1 KIT

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 PACKAGE	0.9 g
Part 2	21 PACKAGE	16.8 mL
Part 3	1 BOTTLE	10 mL
Part 4	6 PACKAGE	3 mL
Part 5	2 PACKAGE	1 mL
Part 6	2 PACKAGE	4
Part 7	2 TUBE	1 g

Part 1 of 7

GENUINE FIRST AID BURN ANTISEPTIC PAIN RELIEF WITH ALOE 
benzalkonium chloride, lidocaine cream

Product Information
Item Code (Source)	NDC: 52124-0004
Route of Administration	TOPICAL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0004-1	0.9 g in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part345	04/27/2010

Part 2 of 7

ANTISEPTIC TOWELETTE 
benzalkonium chloride liquid

Product Information
Item Code (Source)	NDC: 52124-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.40 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0001-1	0.8 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333	04/27/2010

Part 3 of 7

STERILE ISOTONIC BUFFERED GENUINE EYEWASH 
water liquid

Product Information
Item Code (Source)	NDC: 52124-0005
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	98.16 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
EDETATE DISODIUM (UNII: 7FLD91C86K)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0005-1	10 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	04/27/2010

Part 4 of 7

ALCOHOL CLEANSING PAD 
isopropyl alcohol liquid

Product Information
Item Code (Source)	NDC: 52124-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0002-1	0.5 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333	04/27/2010

Part 5 of 7

INSECT STING RELIEF PAD 
benzocaine,alcohol liquid

Product Information
Item Code (Source)	NDC: 52124-0008
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5)	BENZOCAINE	6 mL  in 100 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0008-1	0.5 mL in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part348	04/27/2010

Part 6 of 7

CHEWABLE ASPIRIN 
aspirin tablet, chewable

Product Information
Item Code (Source)	NDC: 52124-0012
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E)	ASPIRIN	81 mg

Inactive Ingredients
Ingredient Name	Strength
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
SACCHARIN (UNII: FST467XS7D)
SODIUM CATION (UNII: LYR4M0NH37)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STARCH, CORN (UNII: O8232NY3SJ)
STEARIC ACID (UNII: 4ELV7Z65AP)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	orange (ORANGE)	Score	no score
Shape	ROUND	Size	11mm
Flavor		Imprint Code	ASPIRIN
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0012-1	2 in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part345	04/27/2010

Part 7 of 7

GENUINE TRIPLE ANTIBIOTIC 
bacitracin zinc,neomycin sulfate,polymyxin b sulfate ointment

Product Information
Item Code (Source)	NDC: 52124-0003
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	5 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B SULFATE	5000 [iU]  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52124-0003-1	0.5 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333	04/27/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333	04/27/2010

Labeler - Acme United Corp. (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
GFA Production ( Xiamen) Co., Ltd		421256261	manufacture