Label: AMERICAN RED CROSS FIRST AID KIT - alcohol, benzalkonium chloride, bacitracin zinc, neomycin sulfate, polymyxin b sulfate, alcohol

  • NDC Code(s): 42354-7482-4, 52124-0001-1, 52124-0002-1, 52124-0003-1, view more
    52124-2906-1
  • Packager: Tomy International
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 January 17, 2012

If you are a consumer or patient please visit this version.

  • Active Ingredient



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

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  • Use

        For preparation of skin before injection.

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  • Warnings

    For external use only.

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  • STORAGE AND HANDLING

    Flammable - keep away from fire or flame

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

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  • Do not use:

    with electrocautery, in the eyes.

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  • STOP USE

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

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  • Keep out of reach of children

    If swallowed,

    get medical help or contact a Poison Control

    Center right away.

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  • WHEN USING

    Wipe Injection site vigorously and discard.

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  • Inactive Ingredient

    Purified water.

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  • DESCRIPTION

    LOT/EXP:                Made in CHINA

    20140301

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  • PRINCIPAL DISPLAY PANEL

    Alcohol Cleansing  Pad
    Genuine First Aid LLC, Clearwater FL 33755

    www.GenuineFirstAid.com

    1/pouch

    GENUINE FIRST AID

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  • Active Ingredient

    Bacitracin Zinc 400 units

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

    Polymyxin B Sulfate 5000 units

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  • Uses:

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

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  • Warnings>

    For external use only.

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  • 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.

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  • Stop use and consult a doctor

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

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  • Keep out of reach of children

    If ingested, contact a Poison

    Control Center right away.

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  • Directions

    Cclean 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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  • Other Information

    Store at room temperature.

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  • 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.

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  • Active Ingredint

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

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  • Use

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

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  • Warning

    For external use only.

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  • Keep out of reach of children

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

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  • STOP USE

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

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  • DO NOT USE

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

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  • 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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  • Inactive Ingredient

    Purified water


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  • DESCRIPTION

    LOT/EXP:                           Made in CHINA

    20130301

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  • Active Ingredient

    Ethyl Alcohol 62%

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  • Purpose

    Antimicrobial

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  • Uses

    For handwashing to decrease bacteria on the skin.

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  • Warnings

    For external use only.

    Flammable

    Do not use

    in the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and consult a doctor


    if irritation and redness develop and persist for more than 72 hours
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  • Directions

    Empty contents into palm. Rub hands until gel dissipates. Recommended for repeated use.

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  • Inactive Ingredients

    Propylene glycol, carbomer, titanium dioxide, purified water

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  • Keep out of reach of children

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

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  • PRINCIPAL DISPLAY PANEL

    Genuine Hand Sanitizer

    Instant Gel

    Antiseptic Handwash with Vitamin E and Aloe

    Kills 99.9% of germs without water

    Active Ingredient:

    Ethyl alcohol 62%

    Net Wt 0.9g (1/32oz)

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  • PRINCIPAL DISPLAY PANEL

    Antiseptic Towelette

    Genuine First Aid LLC, Clearwater FL 33755

    www.GenuineFirstAid.com

    1/pouch

    GENUINE FIRST AID

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  • INGREDIENTS AND APPEARANCE
    AMERICAN RED CROSS FIRST AID KIT 
    alcohol, benzalkonium chloride, bacitracin zinc, neomycin sulfate, polymyxin b sulfate, alcohol kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:42354-7482
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:42354-7482-4 1 in 1 KIT
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 2 TUBE 1.0 g
    Part 2 2 PACKAGE 1.6 mL
    Part 3 4 PACKAGE 2.0 mL
    Part 4 2 PACKET 1.8 g
    Part 1 of 4
    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
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52124-0003-1 .5 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333B 01/11/2011
    Part 2 of 4
    ANTISEPTIC TOWELETTE 
    benzalkonium chloride swab
    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 part333E 01/11/2011
    Part 3 of 4
    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 not final part333A 01/11/2011
    Part 4 of 4
    GENUINE HAND SANITIZER 
    alcohol gel
    Product Information
    Item Code (Source) NDC:52124-2906
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52124-2906-1 0.9 g in 1 PACKET
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 03/28/2011
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 01/17/2012
    Labeler - Tomy International (065183758)
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