Label: READY CARE KIT- first aid kit kit

  • NDC Code(s): 59898-740-01, 59898-902-01, 65517-0001-1, 65517-0004-1, view more
    65517-0020-1
  • Packager: Dukal Corporation
  • Category: MEDICAL DEVICE
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

Drug Label Information

Updated September 23, 2010

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

  • PRINCIPAL DISPLAY PANEL

    Physicians Care

    FIRST AID

    25 Person

    ReadyCare Kit

    Contains over 182 Pieces


  • Back Label

    Physicians Care

    CLEANSE

    Antiseptics

    14    Antiseptic Wipes
    16    Alcohol Pads

    TREAT

     6     Antibiotic Ointment Packets
     6     Burn Ointment Packets
    10    3" Cotton Tip Applicator

    PROTECT

    16     3/8” x 1 1/2” Bandages
    16     1” x 3” Bandages
    80     3/4” x 3” Bandages
    1      1/2" Tape
    1      Triangular Bandage
    4      3" x 3" Sterile Gauze Pads
    1      Abdominal Compress

    Other

    Medical Exam Latex Gloves (2 Pair)
    1       Tweezers
    1       Cold Pack
    1       First Aid Guide
    10     Finger Splints


    Acme United Corporation
    60 Round Hill Road
    Fairfield CT 06824

    www.acmeunited.com

    Designed in the USA | Made in China

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

  • BZK Towelette Labeling

    Reorder 855

    NDC 65517-0004-1

    Dukal

    BZK TOWELETTE

    Contains Benzalkonium Chloride

    For External Use Only

    Helps Prevent Infection

    1 / Pouch

    DUKAL CORPORATION

    (631) 656-3800

    Ronkonkoma, NY 11779 www.dukal.com

    Made in China


    Drug Facts

    Active Ingredients..................... Benzalkonium Chloride 0.133% w/v

    Purpose................................. First Aid Antiseptic

    USE: Antiseptic Cleansing of face, hands and
    body without soap and water. Airs dries in seconds

    DO NOT USE: in the eyes or apply over large
    areas of the body.

    STOP USE: If irritation, redness or other symptoms
    develop. Consult a doctor if the conditions persists
    or gets worse.

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

    DIRECTIONS: Tear open packet, unfold and use
    as a washcloth.

    INACTIVE INGREDIENTS: Distilled Water


  • Prep Pad Labeling

    Reorder 852

    Dukal Corporation

    NDC 65517-0001-1

    NPN 80003156

    ALCOHOL PREP PAD

    Saturated with 70% Isopropyl Alcohol

    For External Use Only

    1 / Pouch

    Dukal Corporation

    Ronkonkoma, NY 11779

    631-656-3800

    www.dukal.com

    Made in China


    Drug Facts

    Active Ingredients

    Isopropyl Alcohol 70%

    Purpose

    Antiseptic Cleanser

    Use

    For Preparation of 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 and 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

  • Ready Care Kit Front Label

    Front Label

  • Ready Care Kit Back Label

    Back Label

  • Prep Pad Label

    Prep Pad Label

  • BZK Towelette Label

    Antiseptic Towelette Label

  • Triple Antibiotic Label

    Triple Antibiotic Label

  • Burn Cream Label

    Burn Cream Label

  • INGREDIENTS AND APPEARANCE
    READY CARE KIT 
    first aid kit kit
    Product Information
    Product TypeMEDICAL DEVICEItem Code (Source)NDC:65517-0020
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65517-0020-11 in 1 PACKAGE, COMBINATION
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 116 POUCH 6.4 mL
    Part 26 PACKET 5.4 g
    Part 36 PACKET 5.4 g
    Part 414 POUCH 19.6 mL
    Part 1 of 4
    DUKAL ALCOHOL PREP PAD 
    isopropyl alcohol swab
    Product Information
    Item Code (Source)NDC:65517-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.70 mL  in 1.0 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65517-0001-10.4 mL in 1 POUCH
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/2000
    Part 2 of 4
    WATER-JEL 3-IN1 ANTIBIOTIC 
    bacitracin zinc, polymyxin b sulfate and neomycin sulfate ointment
    Product Information
    Item Code (Source)NDC:59898-740
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC400 [iU]  in 1 g
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE3.5 mg  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B SULFATE5000 [iU]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59898-740-010.9 g in 1 PACKET
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33301/01/2010
    Part 3 of 4
    FIRST AID BURN 
    lidocaine hydrochloride and benzalkonium chloride cream
    Product Information
    Item Code (Source)NDC:59898-902
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE0.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59898-902-010.9 g in 1 PACKET
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33301/01/2010
    Part 4 of 4
    BZK TOWELETTE 
    benzalkonium chloride swab
    Product Information
    Item Code (Source)NDC:65517-0004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.00186 mL  in 1.4 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 1.39814 mL  in 1.4 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65517-0004-11.4 mL in 1 POUCH
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/2006
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33305/01/2010
    Labeler - Dukal Corporation (791014871)