Label: 4385 FIRST AID KIT- 4385 first aid kit

  • NDC Code(s): 0498-0100-02, 0498-0121-00, 0498-0143-04, 0498-4385-01
  • Packager: Honeywell Safety Products USA, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 22, 2024

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

  • Eyewash Active ingredient

    Sterile Water 99%

  • Eyewassh Purpose

    Eyewash

  • Eyewash Uses

    • for flushing the eye to remove loose foreign material, air pollutants or chlorinated water
  • Eyewash Warnings

    For external use only

    • Obtain immediate medical treatment for all open wounds in or near eyes.
    • To avoid contamination, do not touch tip of container to any surface.
    • Do not reuse.
    • Once opened, discard.

    Do not use

    • if solution changes color or becomes cloudy
    • if you have open wounds in or near the eyes, get medical help right away.

    Stop use and ask a doctor if

    • you experience eye pain
    • changes in vision
    • continued redness or irritation of the eye
    • condition worsens or persists

    Keep out of reach of children

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

  • Eyeash Directions

    • remove contacts before using
    • twist top to remove
    • flush the affected area as needed
    • control rate of flow by pressure on the bottle
    • if necessary, continue flushing with emergency eyewash or shower
  • Eyewash Inactive ingredients

    sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

  • Eyeash Questions

    Call 1-800-430-5490 Honeywell Safety Products USA, Inc. Smithfield, RI 02917

  • Isotonic Solution for Irrigation.

    For Irrigation Only.

    Not for Injection.

  • Description NaCL Irrigation


    Each 100 mL contains:
    Sodium Chloride USP 0.9 g; Water for Injection USP qs

    pH adjusted with Hydrochloric Acid NF
    pH: 5.0 (4.5–7.0) Calculated Osmolarity: 310 mOsmol/liter

    Concentration of Electrolytes (mEq/liter): Sodium 154; Chloride 154
    0.9% Sodium Chloride Irrigation USP is sterile, nonpyrogenic, isotonic and contains no bacteriostatic or antimicrobial agents.

    The formula of the active ingredient is:
    Ingredient Molecular Formula Molecular Weight
    Sodium Chloride USP NaCl 58.44

    The plastic container is a copolymer of ethylene and propylene formulated and developed for parenteral drugs. The copolymer contains no plasticizers and exhibits virtually no leachability. The plastic container is also virtually impermeable to vapor transmission and, therefore, requires no overwrap to maintain the proper drug concentration. The safety of the plastic container has been confirmed by biological evaluation procedures. The material passes Class Vl testing as specified in the U.S. Pharmacopeia for Biological Tests — Plastic Containers. These tests have shown that the container is nontoxic and biologically inert.

    The PIC™ Container is PVC-free and DEHP-free.


    Ingredient Molecular Formula Molecular Weight
    Sodium Chloride USP NaCl 58.44

    The plastic container is a copolymer of ethylene and propylene formulated and developed for parenteral drugs. The copolymer contains no plasticizers and exhibits virtually no leachability. The plastic container is also virtually impermeable to vapor transmission and, therefore, requires no overwrap to maintain the proper drug concentration. The safety of the plastic container has been confirmed by biological evaluation procedures. The material passes Class Vl testing as specified in the U.S. Pharmacopeia for Biological Tests — Plastic Containers. These tests have shown that the container is nontoxic and biologically inert.

    The PIC™ Container is PVC-free and DEHP-free.

  • Clinical Pharmacology NaCL Irrigant

    0.9% Sodium Chloride Irrigation USP is utilized for a variety of clinical indications such as sterile irrigation of body cavities, tissues or wounds, indwelling urethral catheters, surgical drainage tubes, and for washing, rinsing or soaking surgical dressings, instruments and laboratory specimens. It also serves as a diluent or vehicle for drugs used for irrigation or other pharmaceutical preparations.

    0.9% Sodium Chloride Irrigation USP provides an isotonic saline irrigation identical in composition with 0.9% Sodium Chloride Injection USP (normal saline).

    Physiological irrigation solutions are considered generally compatible with living tissues and organs.

    Sodium, the major cation of the extracellular fluid, functions primarily in the control of water distribution, fluid balance, and osmotic pressure of body fluids. Sodium is also associated with chloride and bicarbonate in the regulation of the acid-base equilibrium of body fluid.

    Chloride, the major extracellular anion, closely follows the metabolism of sodium, and changes in the acid-base balance of the body are reflected by changes in the chloride concentration.

  • Indication and Usage NaCl Irrigant

    0.9% Sodium Chloride Irrigation USP is indicated for all general irrigation, washing, rinsing and dilution purposes which permit use of a sterile, nonpyrogenic electrolyte solution.

  • Contraindications NaCl Irrigant

    0.9% Sodium Chloride Irrigation USP is not for injection by usual parenteral routes.

    An electrolyte solution should not be used for irrigation during electrosurgical procedures.

  • Warnings NaCl Irrigant

    FOR IRRIGATION ONLY. NOT FOR INJECTION.

    Irrigating fluids have been demonstrated to enter the systemic circulation in relatively large volumes; thus, irrigation solutions must be regarded as systemic drugs. Absorption of large amounts can cause fluid and/or solute overload resulting in dilution of serum electrolyte concentrations, overhydration, congested states or pulmonary edema.

    The risk of dilutional states is inversely proportional to the electrolyte concentrations of the administered parenteral solutions. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentration.

    Do not warm above 150°F (66°C).

    After opening container, its contents should be used promptly to minimize the possibility of bacterial growth or pyrogen formation.

    Discard unused portion of irrigating solution since it contains no preservatives.

  • Precautions NaCl Irrigant

    General
    Use aseptic technique when preparing and administering sterile irrigation solutions.

    Use only if solution is clear and container and seal are intact.

    Do not use for irrigation that may result in absorption of large amounts of fluid into the blood.

    Caution should be observed when the solution is used for continuous irrigation or allowed to "dwell" inside body cavities because of possible absorption into the blood stream and the production of circulatory overload.

    When used for irrigation via appropriate irrigation equipment, the administration set should be attached promptly. Unused portions should be discarded and a fresh container of appropriate size used for the start up of each cycle or repeat procedure. For repeated irrigations of urethral catheters, a separate container should be used for each patient.

    Laboratory Tests

    Clinical evaluation and periodic laboratory determinations are necessary to monitor changes in fluid balance, electrolyte concentrations, and acid-base balance after prolonged irrigation, when fluid absorption is suspected, or whenever the condition of the patient warrants such evaluation.

    Drug Interactions

    Some additives may be incompatible. Consult with pharmacist.When introducing additives, use aseptic technique.Mix thoroughly.

    Do not store.


    Carcinogenesis, Mutagenesis, Impairment of Fertility

    Studies with 0.9% Sodium Chloride Irrigation USP have not been performed to evaluate carcinogenic potential, mutagenic potential, or effects on fertility.

    Pregnancy

    Teratogenic Effects

    Animal reproduction studies have not been conducted with 0.9% Sodium Chloride Irrigation USP. It is also not known whether 0.9% Sodium Chloride Irrigation USP can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. 0.9% Sodium Chloride Irrigation USP should be given to a pregnant woman only if clearly needed.

    Labor and Delivery

    Safety and effectiveness of 0.9% Sodium Chloride Irrigation USP during labor and delivery have not been established. Caution should be exercised, and the fluid balance, glucose and electrolyte concentrations, and acid-base balance, of both mother and fetus should be evaluated periodically or whenever warranted by the condition of the patient or fetus.

    Nursing Mothers

    It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when 0.9% Sodium Chloride Irrigation USP is administered to a nursing woman.

    Pediatric Use

    The safety and effectiveness of 0.9% Sodium Chloride Irrigation USP in pediatric patients have not been established. Its limited use in pediatric patients has been inadequate to fully define proper dosage and limitations for use.

    Geriatric Use

    Clinical studies of 0.9% Sodium Chloride Irrigation USP did not include a sufficient number of patients age 65 years and over to determine whether they respond differently from younger subjects. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.

    This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function.Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.Frequent laboratory determinations and clinical evaluations are recommended to monitor changes in blood glucose, electrolyte concentrations, and renal function.

  • Adverse Reactions

    Possible adverse effects arising from the irrigation of body cavities, tissues, or indwelling catheters and tubes can be minimized when proper procedures are followed. Displaced catheters or drainage tubes can lead to irrigation or infiltration of unintended structures or cavities. Excessive volume or pressure during irrigation of closed cavities may cause undue distension or disruption of tissues. Accidental contamination from careless technique may transmit infection.

    If an adverse reaction does occur, discontinue administration of the irrigant, evaluate the patient, institute appropriate therapeutic countermeasures, and save the remainder of the fluid for examination if deemed necessary.

  • Overdosage

    In the event of overhydration or solute overload, reevaluate the patient's condition, and institute appropriate corrective treatment. Intravasular volume overload may respond to hemodialysis. See WARNINGS, PRECAUTIONS, and ADVERSE REACTIONS.

  • Dosage and Administration

    As required for irrigation.

    When used as a diluent, or vehicle for other drugs, the drug manufacturer's recommendations should be followed.

    Some additives may be incompatible. Consult with pharmacist. When introducing additives, use aseptic techniques. Mix thoroughly. Do not store.

    Solutions should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permits.

  • How Supplied

    0.9% Sodium Chloride Irrigation USP is supplied sterile and nonpyrogenic in PIC™ (Plastic Irrigation Container). The 1000 mL and 500 mL containers are packaged 16 per case, the 2000 mL containers are packaged 8 per case, and the 4000 mL containers are packaged 4 per case.

    0.9% Sodium Chloride Irrigation USP


    NDC Cat. No. REF SIZE

    0264-2201-00 R5200-01 1000 mL
    0264-2201-10 R5201-01 500 mL
    0264-2201-50 R5205-01 2000 mL
    0264-2201-70 R5207 ,,,,4000 mL

    Exposure of pharmaceutical products to heat should be minimized. Avoid excessive heat. Protect from freezing. It is recommended that the product be stored at room temperature (25°C); however, brief exposure up to 40°C does not adversely affect the product.

    Do not warm above 150°F (66°C).

  • SPL Unclassified Section

    Rx only

    Revised: March 2009

    PIC is a trademark of B. Braun Medical Inc.

  • DIRECTIONS FOR USE OF PIC™ (PLASTIC IRRIGATION CONTAINER)

    Not for injection.

    Aseptic technique is required.

    Caution – Before use, perform the following checks:

    (a) Read the label. Ensure solution is the one ordered and is within the expiration date.

    (b) Invert container and inspect the solution in good light for cloudiness, haze, or particulate matter; check the
    container for leakage or damage. Any container which is suspect should not be used.

    Use only if solution is clear and container and seal are intact

    Single unit container. Discard unused portion.
    Outer Closure Removal – Grasp the container with one hand and turn the breakaway ring counterclockwise with the other hand until slight resistance is felt. Then, twisting the container in the opposite direction, turn the breakaway ring sharply until the entire outer cap is loose and can be lifted off.

    Fig. 1

    Figure 1

    Connect the administration set through the sterile set port according to set instructions or remove screw cap and pour.

    [Fig 2]

    Fig 2

    Figure 2

    Do not warm above 150°F (66°C) to assure minimal bottle distortion. Keep bottles upright.

  • SPL Unclassified Section

    B. Braun Medical Inc.
    Irvine, CA 92614-5895 USA
    Made in USA

    Y36-002-699

  • Alcohol Wipe Active ingredient

    Isopropyl alcohol 70%

  • Alcohol Wipe Purpose

    First aid antiseptic

  • Alcohol Wipe Uses

    first aid to help prevent infection in minor cuts, scrapes, and burns

  • Alcohol Wipe Warnings

    For external use only

    Flammable, keep away from fire and flame

    Do not use

    • in or near eyes
    • over large areas of the body

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    When using this product

    • do not use longer than 1 week unless directed by a doctor

    Stop use and consult a doctor if

    • condition persists or gets worse

    Keep out of the reach of children

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

  • Alcohol Wipe Directions

    • clean the affected area
    • may be covered with a sterile bandage
    • apply wipe to affeted are 1 to 3 times daily
    • discard wipe after single use
  • Alcohol Wipe Other information

    • store at room temperature 15 o to 25 0 C (59 0 to 77 0 oF)
    • do not use if packet is torn or opened
  • Alcohol Wipe Inactive ingredients

    water

  • Alcohol Wipe Questions

    1-800-430-5490

  • PVP Wipes Active ingredients

    Povidone-iodine 10%

    (equivalent to 1% titratable iodine)

  • PVP Wipes Purpose

    First aid antiseptic

  • PVP Wipes Uses

    • first aid antiseptic to help prevent infection in minor cuts, scrapes and burns
  • PVP Wipes Warnings

    For external use only.

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if

    • condition worsens or persists for more than 72 hours
    • irritation and redness develops

    Keep out of reach of children.

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

  • PVP Wipes Directions

    • clean the affected area
    • apply1 to 3 times daily
    • may be covered with a sterile bandage
    • if bandaged, let dry first
    • discard wipe after single use
  • PVP Wipes Other Information

    • do not use on individuals who are allergic or sensitive to iodine
    • store at controlled temperature 59-86ºF (15-30ºC)
    • do not use if pouch is open or torn
  • PVP Wipes Inactive ingredients

    nonoxynol 9, water

  • PVP Wipes Questions

    1-800-430-5490

  • PAWS Active ingredient

    Ethyl alcohol 66.5%

  • PAWS Purpose

    Antiseptic

  • PAWS Uses

    • for handwashing to decrease bacteria on skin whenever soap and water is not readily available
  • PAWS Warnings

    For external use only

    Flammable: keep away from fire or flame

    Do not use in the eyes.

    If this happens, rinse thoroughly with water.

    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

  • PAWS Directions

    • wet hands and wrists thoroughly for 15 seconds and allow to air dry
    • always reseal after use
    • children under 6 years of age should be supervised when using this product
  • PAWS Inactive ingredients

    aloe vera, fragrance, purified water, triethanolamine

  • PAWS Questions

    1-800-430-5490

  • 4385 346100 Kit Contents

    1 ALCOHOL PREP PADS 10P

    1 PVP IODINE WIPES 10 PER

    1 NITRILE GLOVES 2PR BBP

    1 O/H TAPE ADHESIVE TRI-CUT

    1 BK GZ 4.5"X4.1YD6PLY RL ST MSO

    1 FIRST AID GUIDE ASHI

    1 EMERGENCY SURVIVAL BLANKET

    2 GAUZE CLEAN-WRAP BDGE N/S 2"

    1 BLOODSTOPPER

    2 ABD COMBINE PAD 5" X 9"

    2 ABD PADS 8"X10" STERILE

    1 SOD. CHLORIDE 0.9% 500ML EA

    1 4OZ BFS EYEWASH TRILINGUAL BOTTLE

    1 EMPTY BAG RED 8X8X6

    1 LBL STOCK 6-3/8"X4"

    1 LBL STOCK 4"X2-7/8"

    1 LBL STOCK 3"x1-7/8"

    1 POLY BAG, 19 X 24 (CLEAR)

    1 BANDAGE PACK FOR KIT

    1 ZIP LOCK BAG FOR KIT #3

    1 SELF-ADH WRAP 3 X 5 YDS NORTH REV E

    1 WATER-JEL BURN DRESSING 4 X 4

    1 CORRUGATED 24PK 01-0810 RSC

    1 TRI BNDG NON WOVEN 40"X40"X56"

    1 COLD PACK UNIT 4"X6" BULK

    1 CPR MSK,PAWS WPS,GLVS 1

  • Eyewash Principal Display Panel

    Eyesaline

  • Principal Display Panel 500 ml Container

    NaCL Irrigation USP

  • Alcohol Wipe Principal Display Panel

    Alcohol Preps

  • PVP Wipes Principal Display Panel

    PVP Wipe

  • PAWS Principal Display Panel

    Paws

  • 4385 Kit Label 346100

    4385 label

  • INGREDIENTS AND APPEARANCE
    4385 FIRST AID KIT 
    4385 first aid kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-4385
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-4385-011 in 1 KIT09/13/2018
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 12 PACKET 0.0038 L
    Part 210 POUCH 3 mL
    Part 31 BOTTLE 118 mL
    Part 410 POUCH 4 mL
    Part 51 CONTAINER 500 mL
    Part 1 of 5
    PAWS 
    ethyl alcohol liquid
    Product Information
    Item Code (Source)NDC:0498-3111
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL665 mL  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    10.0019 L in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/21/2017
    Part 2 of 5
    PVP IODINE WIPE 
    povidone-iodine 10% swab
    Product Information
    Item Code (Source)NDC:0498-0121
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    NONOXYNOL-9 (UNII: 48Q180SH9T)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0121-000.3 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/18/2018
    Part 3 of 5
    EYESALINE EMERGENCY EYEWASH 
    purified water liquid
    Product Information
    Item Code (Source)NDC:0498-0100
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER98.6 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0100-02118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01812/18/2018
    Part 4 of 5
    ALCOHOL WIPE 
    isopropyl alcohol swab
    Product Information
    Item Code (Source)NDC:0498-0143
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0143-040.4 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/18/2018
    Part 5 of 5
    SODIUM CHLORIDE 
    sodium chloride irrigant
    Product Information
    Item Code (Source)NDC:0264-2201
    Route of AdministrationIRRIGATION
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE0.9 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1500 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/14/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/13/2018
    Labeler - Honeywell Safety Products USA, Inc. (118768815)