Label: ACME FIRST AID CONTAINS 404 PIECES - benzalkonium chloride, lidocaine, water, isopropyl alcohol, aspirin, benzocaine, alcohol, bacitracin zinc, neomycin sulfate, polymyxin b sulfate
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NDC Code(s):
0924-1806-01,
52124-0001-1,
52124-0002-1,
52124-0003-1,
view more52124-0004-1, 52124-0005-1, 52124-0008-1, 52124-0012-1
- Packager: Acme United Corp.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 7, 2010
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
Purpose: First aid antiseptic, external analgesic
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Uses: First aid to help prevent infection and for the temporary relief of pain and itching associated with:
Minor Cuts
Scrapes
Burns - WARNINGS
- 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
Close - KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
Directions: Clean affected area, Apply small amount not more than 3 times daily.
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May be covered with a sterile bandage. - STORAGE AND HANDLING
- PRINCIPAL DISPLAY PANEL
Genuine First Aid Burn Cream
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Antiseptic Pain Relief With Aloe
Net Wt 0.9g (1/32 oz)
Manufactured in CHINA for
Genuine First Aid. - ACTIVE INGREDIENT
- PURPOSE
Use: For Professional and Hospital use. Helps prevent infection. Antiseptic cleansing of face, hands and body without soap and water.
Close - WARNINGS
- 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.
Close - STOP USE
Stop use if unusual redness, swelling or other symptoms occur. Consult a physician immediately.
Close - DO NOT USE
- WHEN USING
Directions: Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appropriately after single use.
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- DESCRIPTION
- PRINCIPAL DISPLAY PANEL
Antiseptic Towelette
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Genuine First Aid LLC, Clearwater FL 33755
www.GenuineFirstAid.com
1/pouch
GENUINE FIRST AID - ACTIVE INGREDIENT
Active Ingredient: .........Bacitracin Zinc 400 units
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Neomycin Sulfate 5mg ( equivalent to 3.5 mg Neomycin base)
Polymyxin B Sulfate 5000 units - PURPOSE
- WARNINGS
- DO NOT USE
Do not use: in eyes; over large areas of the body;
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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:
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if the condition persists or gets worse; a rash or other allergic reaction develops - KEEP OUT OF REACH OF CHILDREN
- 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
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- PRINCIPAL DISPLAY PANEL
Genuine Triple Antibiotic
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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. - ACTIVE INGREDIENT
- INACTIVE INGREDIENT
Inactive Ingredients:
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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.
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Discard unused portion of the solution.
Not for injection. - WARNINGS
Warning:
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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:
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For flushing or irrigating the eyes to
remove loose foreign material, air pollutants,
or chlorinated water. - DESCRIPTION
- PRINCIPAL DISPLAY PANEL
- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- STORAGE AND HANDLING
Flammable - keep away from fire or flame
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Store at room temperature 15-30 degree Celsius (59-86 degree Fahrenheit) - DO NOT USE
- STOP USE
Stop use if irritation and redness develop. If condition persists for more than 72 hours, consult your doctor.
Close - KEEP OUT OF REACH OF CHILDREN
Keep out of reach of children. If swallowed,
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get medical help or contact a Poison Control
Center right away. - WHEN USING
- INACTIVE INGREDIENT
- DESCRIPTION
- PRINCIPAL DISPLAY PANEL
Alcohol Cleansing Pad
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Genuine First Aid LLC, Clearwater FL 33755
www.GenuineFirstAid.com
1/pouch
GENUINE FIRST AID - ACTIVE INGREDIENT
Active Ingredient: Purpose:
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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.
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Warnings: For external use only.
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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.
Close - STORAGE AND HANDLING
- 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.
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- PRINCIPAL DISPLAY PANEL
Insect Sting Relief Pad
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Genuine First Aid LLC, Clearwater FL 33755
www.GenuineFirstAid.com
1/pouch
GENUINE FIRST AID - ACTIVE INGREDIENT
Active ingredient (in each tablet) Purpose
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Aspirin 81 mg (NSAID*). . . . . . . . . . . . . Analgesic/Antipyretic
*nonsteroidal anti-inflammatory drug - PURPOSE
Uses
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temporary relief of minor aches, pains and headaches
to reduce fever associated with colds, sore throats, teething - WARNINGS
Warnings
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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
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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;
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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;
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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.
Close - 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.
Close - DOSAGE & ADMINISTRATION
Directions Do not use more than directed
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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
- INACTIVE INGREDIENT
Inactive ingredients flavor, FD and C yellow No. 6, saccharin, sodium, silicon dioxide, starch, stearic acid, sucrose
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MADE IN USA
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Distributed by GENUINE FIRST AID
600 Cleveland Str Suite 400, Clearwater, FL 33755 - PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
PhysiciansCARE
FIRST AID
all purpose kit
with 6 First Aid Pockets1 Small Cuts and Burns
2 Medium Cuts and Scratches
3 Severe Bleeding and Burns
4 CPR
5 Protection
6 InstrumentsNew
REFILL PACKS AVAILABLE FOR EACH POCKETHOME 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 BarrierPROTECTION 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
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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 - 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 kitProduct 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 creamProduct 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 liquidProduct 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 liquidProduct 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 liquidProduct 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 liquidProduct 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, chewableProduct 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 ointmentProduct 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