Label: ADVENTURE FIRST AID .5 TIN- benzocaine, alcohol, benzalkonium chloride

  • NDC Code(s): 44224-0203-1, 52124-0001-1, 52124-0003-1, 52124-0008-1, view more
    52124-0017-1
  • Packager: Tender Corporation
  • 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 March 16, 2017

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

  • Active Ingredient - Antiseptic

    Benzalkonium Chloride 0.13%

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  • Purpose - Antiseptic

    Antiseptic

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  • Use - Antiseptic

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

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  • Warnings, Precautions and Directions - Antiseptic

    For External use only.

    Keep out of Reach of Children.

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

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

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

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  • Inactive Ingredients - Antiseptic

    Purified Water

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  • Active Ingredient - Alcohol Prep Pad

    Isopropyl Alcohol 70%

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  • Use - Alcohol Prep Pad

    For preparation of the skin before injection

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  • Warnings, Precautions and Directions - Alcohol Prep Pad

    For External Use Only

    Flammable - Keep away from fire or flame

    Do Not Use - with electrocautery, in eyes

    Stop Use and Ask a Doctor if - Irritation or redness develop and persists for more than 72 hours

    Keep out of Reach of Children

    If swallowed, get medical help or contact a poison control center right away.

    Tear Open packet, unfold and use as and wipe injection site vigorously and discard.

    Store at Room Temperature

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  • Active Ingredients - Insect Relief Pad

    Benzocaine 6%

    SD alcohol 60%

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  • Purpose - Insect Relief Pad

    Topical Anesthetic - Antiseptic

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  • Use - Insect Relief Pad

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

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  • Warnings, Precautions and Directions - Insect Relief Pad

    Clean intended area thoroughly with pad. Discard after single use

    Warnings: For external use only.

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

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

    Flammable - keep away from fire or flame

    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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  • Active Ingredients - Triple Antibiotic Ointment

    Bacitracin Zinc 400 units

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

    Polymyxin B Sulfate 5000 units

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  • Purpose - Triple Antibiotic Ointment

    Triple Antibiotic

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  • Use - Triple Antibiotic Ointment

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

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  • Warnings, Precautions and Directions - Triple Antibiotic Ointment

    For external use only.

    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 and consult 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 a Poison Control Center right away

    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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  • Adventure First Aid .5 Tin
  • INGREDIENTS AND APPEARANCE
    ADVENTURE FIRST AID .5 TIN 
    benzocaine, alcohol, benzalkonium chloride kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:44224-0203
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:44224-0203-1 1 in 1 BOX; Type 0: Not a Combination Product 10/01/2015
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 2 PACKAGE 1 mL  in .5 
    Part 2 4 PACKAGE 3 mL  in .7 
    Part 3 4 PACKAGE 3 mL  in .8 
    Part 4 4 TUBE 2 g  in .5 
    Part 1 of 4
    INSECT STING RELIEF PAD 
    benzocaine,alcohol swab
    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 0.6 mg  in 100 mL
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 60 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:52124-0008-1 0.5 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part348 04/23/2011
    Part 2 of 4
    ALCOHOL PREP PAD 
    isopropyl alcohol swab
    Product Information
    Item Code (Source) NDC:52124-0017
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 700 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52124-0017-1 0.7 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 02/01/2016
    Part 3 of 4
    ANTISEPTIC 
    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 1.3 mg  in 1 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; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 04/23/2010
    Part 4 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
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 5 mg  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 5000 [iU]  in 1 g
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [iU]  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    PETROLATUM (UNII: 4T6H12BN9U)  
    WATER (UNII: 059QF0KO0R)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:52124-0003-1 0.5 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333B 12/28/2016
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 10/01/2015
    Labeler - Tender Corporation (064437304)
    Registrant - Tender Corporation (064437304)
    Establishment
    Name Address ID/FEI Business Operations
    Tender Corporation 064437304 manufacture(44224-0203)
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