Label: CVS FIRST AID KIT- diphenhydramine hydrochloride, aspirin, isopropyl alcohol, bacitracin zinc, neomycin sulfate, polymyxin b, benzalkonium chloride, ammonia, lidocaine, acetaminophen, ibuprofen, kit

  • NDC Code(s): 44224-0001-2, 52124-0001-1, 52124-0003-1, 52124-0013-1, view more
    52124-0014-1, 52124-0040-1, 69842-200-00
  • Packager: CVS
  • 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 18, 2017

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

  • Active Ingredients - Genuine Triple Antibiotic

    Active Ingredient: .........Bacitracin Zinc 400 units

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

    Polymyxin B Sulfate 5000 units

  • Purpose - Genuine Triple Antibiotic

    Triple Antibiotic

  • Uses - Genuine Triple Antibiotic

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

  • Warnings - Genuine Triple Antibiotic

    For external use only

  • DO NOT USE - Genuine Triple Antibiotic

    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 - Genuine Triple Antibiotic

    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 - Genuine Triple Antibiotic

    Keep out of reach of children.

    If ingested, contact a Poison

    Control Center right away.

  • Directions - Genuine Triple Antibiotic

    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

  • Storage and Handling - Genuine Triple Antibiotic

    Other information:

    Store at room temperature.

  • Inactive Ingredients - Genuine Triple Antibiotic

    Vaseline
    Mineral Oil
    Purified Water

  • Active Ingredients - Antiseptic

    Active Ingredient:

    Benzalkonium Chloride 0.13

  • Purpose - Antiseptic

    Antiseptic

  • Use - Antiseptic

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

  • Warnings - Antiseptic

    Warning: For external use only.

  • Keep out of reach of children - Antiseptic

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

  • Stop Use - Antiseptic

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

  • Do Not Use - Antiseptic

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

  • Directions - Antiseptic

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

  • Inactive Ingredients - Antiseptic

    Inactive Ingredient: Purified water

  • Active Ingredient - Ibuprofen

    Ibuprofen USP (NSAID*) 200mg
    *nonsteroidal anti-inflammatory drug

  • Purpose - Ibuprofen

    Pain reliever/fever reducer

  • Uses - Ibuprofen

    temporarily relieves minor aches and pains due to:

    the common cold

    headache

    toothache

    muscular aches

    backache

    minor pain of arthritis

    menstrual cramps temporarily reduces fever

  • Warnings - Ibuprofen

    Allergy alert : Ibuprofen may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include: shock, facial swelling, asthma (wheezing) rash, skin reddening, blisters, hives If an allergic reaction occurs, stop use and seek medical help right away.

    Stomach bleeding warning: This product contains a nonsteroidal anti-inflammatory drug (NSAID), which may cause severe stomach bleeding. The chance is higher if you: are age 60 or older, have had stomach ulcers or bleeding problems, take a blood thinner (anticoagulant) or steroid drug, take other drugs containing NSAIDs (aspirin, ibuprofen, naproxen, or others), have 3 or more alcoholic drinks every day while using this product, take more or for a longer time than directed

  • Do Not Use - Ibuprofen

    Do not use if you have ever had an allergic reaction to any other pain reliever/fever reducer, right before or after heart surgery.

  • Ask a Doctor - Ibuprofen

    Ask a doctor before use if stomach bleeding warning applies to you; you have a history of stomach problems such as heartburn; you have a high blood pressure, heart disease, liver cirrhosis, or kidney disease; you are taking a diuretic

    Ask a doctore before use if you are taking any other drug containing NSAID (prescription or nonprescription); taking aspirin for heart attack or stroke, because Ibuprofen may decrease this benefit of aspirin; taking any other drug

  • When Using - Ibuprofen

    when using this product take with food or milk if stomach upset occurs

  • Stop Use - Ibuprofen

    Stop use and ask a doctor if you experience any of the following signs of stomach bleeding; feel faint; vomit blood; have bloody or black stools; have stomach pain that does get better; pain gets worse or lasts more than 10 days; fever gets worse or lasts more than 3 days; redness or swelling is present in the painful area; any new symptoms appear

  • Pregnancy or Breast Feeding - Ibuprofen

    If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use ibuprofen during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

  • Keep out of reach of Children - Ibuprofen

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions - Ibuprofen

    do not use more than directed; the smallest effective dose should be used; do not take longer than 10 days, unless directed by a doctor.

    Adults and Children (12 years and older): Take 1 tablet every 4 to 6 hours while symptoms persist. If pain or fever does not respond to 1 tablet, 2 tablets may be used. Do not exceed 6 tablets in 24 hours, unless directed by a doctor.

    Children under 12 years: Do not give to children under 12 years of age.

  • Other Information

    Store at controlled room temperature; avoid excessive heat 40 degree Celsius (104 degree Fahrenheit); tamper evident sealed packets; do not use any opened or torn packets

  • INACTIVE INGREDIENTS - Ibuprofen

    ​cellulose, corn starch, fumed silica gel, hypromellose, lactose, magnesium stearate, polydextrose, polyethylene glycol, povidone, silica, sodium starch glycolate, stearic acid, titanium dioxide, triacetin

  • Active Ingredients - Non-Aspirin

    Acetaminophen 500 mg

  • Purpose - Non Aspirin

    Analgesic/antipyretic

  • Uses - Non Aspirin

    temporary relief of minor aches and pains associated with:

    common cold; headache; toothache; muscular aches; backache; arthritis; menstrual cramps; and reduction of fever

  • Warnings - Non Aspirin

    Liver warning: This product contains acetaminophen.

    Severe liver damage may occur if: adult takes more than 12 tablets in 24 hours, which is the maximum daily amount; child takes more than 5 doses in 24 hours; taken with other drugs containing acetaminophen; adult has 3 or more alcoholic drinks every day while using this product

  • Do Not Use - Non Aspirin

    with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist; for more than 10 days for pain unless directed by a doctor; for more than 3 days for fever unless directed by a doctor

  • Ask a Doctor - Non Aspirin

    Ask a doctor before use if the user has liver disease

    Ask a doctor or pharmacist before use if the user is taking the blood thinning drug warfarin

  • Stop Use - Non Aspirin

    Stop use and ask a doctor if: symptoms do not improve; pain gets worse or lasts for more than 10 days; fever gets worse or lasts for more than 3 days; new symptoms occur; redness or swelling is present; a rare sensitivity reaction occurs

  • Pregnancy - Non Aspirin

    If pregnant or breast-feeding, ask a health professional before use.

  • Keep Out of Reach of Children - Non Aspirin

    Keep out of reach of children. In case of accidental overdose, contact a doctor or Poison Control Center immediately. Prompt
    medical attention is critical for adults as well as for children even if
    you do not notice any signs or symptoms. Do not exceed recommended dosage

  • Inactive Ingredients - Non Aspirin

    Cornstarch, polyethylene glycol, stearic acid, povidone

  • Directions - Non Aspirin

    Directions

    Adults and Children Take 2 tablets every 4 to 6 hours as

    12 years of age needed. Do not take more than 12 tablets

    or older in 24 hours.

    Children 6-11 years Take 1 tablet every 4 to 6 hours as

    of age needed. Do not take more than 5

    tablets in 24 hours.

    Children under 6 Do not use this regular strength product.

    years of age This will provide more than the

    recommended dose (overdose) and could

    cause serious health problems.

  • Storage and Handling - Non Aspirin

    Store at 59-86 degree F (15-30 degree C)

    tamper evident sealed packets; do not use any open or torn packets

  • Active Ingredients - Burn Cream

    ACTIVE INGREDIENTS:

    Benzalkonium Chloride 0.13%
    Lidocaine HCL 0.5%

  • Purpose - Burn Cream

    Purpose: First aid antiseptic, external analgesic

  • Uses - Burn Cream

    First aid to help prevent infection and for the temporary relief of pain and itching associated with:

    Minor Cuts

    Scrapes

    Burns

  • Warnings - Burn Cream

    For external use only

  • Do Not Use - Burn Cream

    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

    Do not use:
    in the eyes or apply over large areas of the body.
    longer than 1 week unless directed by a doctor.
    in large quantities, particularly over raw surfaces or blistered areas.

    Ask a doctor before use if you have deep puncture wounds, animal bites or serious burns.

    When using this product, avoid contact with the eyes.

  • Stop Use - Burn Cream

    Stop use and ask a doctor if
    condition worsens
    symptoms persist for more than 7 days
    condition clears up and occurs again within a few days

  • Keep Out of Reach of Children

    Keep out of reach of Children.

    If ingested, contact a Poison Control Center right away.

  • Directions - Burn Cream

    Adults and children 2 years of age and older

    clean affected area.

    apply a small amount of this product on the area 1 to 3 times daily.

    may be covered with a sterile bandage

    children under 2 years of age: consult a doctor

  • Storage and Handling - Burn Cream

    Other Information:

    Store at room temperature (do not freeze).

    Taper evident sealed packets.

    Do not use packet if opened or torn.

  • Inactive Ingredients - Burn Cream

    Peregal-O

    Glycerin monostearate

    Glycerol

    Purified Water.

  • Active Ingredients - After Bite

    Active Ingredient:

    Ammonia 3.5%

  • Purpose - After Bite

    Counterirritant

  • Uses - After Bite

    Temporarily protects and helps relieve minor skin irriatation and itching due to

    • insect bites and stings
    • poison ivy, oak or sumac
  • Warnings - After Bite

    Warning: For external use only.

  • Keep Out of Reach of Children - After Bite

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

  • Stop Use - After Bite

    Stop use and ask a doctor if

    • condition worsens
    • symptoms last more than 7 days or clear up and occur again within a few days
  • When Using - After Bite

    Do not get into eyes

  • DIrections - After Bite

    Adults and children under 2 years and older dab directly on bite or sting, rub gently and re-apply as needed

    Children under 2 years ask a doctor

  • First Aid Kit Sleeve

    First Aid Kit

  • Principal Display Panel - Triple Antibiotic

    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.

    Triple Antibiotic

  • Package Label - Antiseptic

    Antiseptic Towelette

    Genuine First Aid LLC, Clearwater FL 33755

    www.GenuineFirstAid.com

    1/pouch

    GENUINE FIRST AID Antiseptic

  • Package Label - Ibuprofen

    Distributed by GENUINE FIRST AID
    600 Cleveland Str Suite 400, Clearwater, FL 33755

    IBUPROFEN 2 Tablets

    Ibuprofen

  • Package Label Non Aspirin

    Non Aspirin

  • Package Label - Burn Cream

    Genuine First Aid Burn Cream

    Antiseptic Pain Relief With Aloe

    Net Wt 0.9g (1/32 oz)

    Manufactured in CHINA for

    Genuine First Aid

    GFA Production Xiamen Co., Ltd
    No. 20 Huli Industrial Park, Meixi Road, Tong'an, Xiamen, Fujian, China 361100
    Tel: 86-592-7269515 Fax: 86-592-7269528 Http: //www.gfaproduction.com

    Burn Cream

  • Package Label - After Bite

    After Bite

    The Itch Eraser

    Fast Relief from Insect Bites.

    Net Contents: 0.037fl. oz.

    Contains: One (1) Wipe

    Contains Ammonia

    Tender Corporation

    Littleton, NH 03561

    After Bite Wipe

  • INGREDIENTS AND APPEARANCE
    CVS FIRST AID KIT 
    diphenhydramine hydrochloride, aspirin, isopropyl alcohol, bacitracin zinc, neomycin sulfate, polymyxin b, benzalkonium chloride, ammonia, lidocaine, acetaminophen, ibuprofen, kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-200
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-200-001 in 1 BAG; Type 0: Not a Combination Product12/28/2016
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 14 PACKAGE 3 mL  in .7 
    Part 22 PACKET 2 g  in .9 
    Part 31 PACKAGE
    Part 41 PACKET
    Part 515 PACKAGE 12 mL  in .8 
    Part 66 TUBE 3 g  in .5 
    Part 1 of 6
    AFTER BITE WIPE 
    ammonia swab
    Product Information
    Item Code (Source)NDC:44224-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE 1000 (UNII: MCU2324216)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    C12-13 ALCOHOLS (UNII: T7ZJT3I9X2)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44224-0001-20.7 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34812/28/2016
    Part 2 of 6
    GENUINE FIRST AID BURN ANTISEPTIC PAIN RELIEF WITH ALOE 
    benzalkonium chloride, lidocaine cream
    Product Information
    Item Code (Source)NDC:52124-0040
    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 HYDROCHLORIDE ANHYDROUS0.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52124-0040-10.9 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/28/2016
    Part 3 of 6
    NON-ASPIRIN 
    acetaminophen tablet
    Product Information
    Item Code (Source)NDC:52124-0014
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    POVIDONE (UNII: FZ989GH94E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize11mm
    FlavorImprint Code AZ;234
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52124-0014-12 in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34312/28/2016
    Part 4 of 6
    IBUPROFEN 
    ibuprofen tablet
    Product Information
    Item Code (Source)NDC:52124-0013
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN200 mg
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYDEXTROSE (UNII: VH2XOU12IE)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TRIACETIN (UNII: XHX3C3X673)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    LACTOSE (UNII: J2B2A4N98G)  
    POVIDONE (UNII: FZ989GH94E)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code 44;352
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52124-0013-12 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07501012/28/2016
    Part 5 of 6
    ANTISEPTIC 
    benzalkonium chloride swab
    Product Information
    Item Code (Source)NDC:52124-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52124-0001-10.8 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/28/2016
    Part 6 of 6
    GENUINE TRIPLE ANTIBIOTIC 
    bacitracin zinc,neomycin sulfate,polymyxin b sulfate ointment
    Product Information
    Item Code (Source)NDC:52124-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 [iU]  in 1 g
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN5 mg  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 [iU]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    WATER (UNII: 059QF0KO0R)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52124-0003-10.5 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333B12/28/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/28/2016
    Labeler - CVS (062312574)
    Establishment
    NameAddressID/FEIBusiness Operations
    Tender Corporation064437304manufacture(69842-200)