Label: EASY CARE FIRST AID KIT - COMPREHENSIVE- ammonia, aspirin, diphenhydramine hydrochloride, ibuprofen, acetaminophen, lidocaine hydrochloride, benzalkonium chloride

  • NDC Code(s): 44224-0001-2, 44224-2999-0, 44224-3300-0, 44224-5120-0, view more
    47682-097-99, 47682-125-99, 47682-184-46, 47682-700-99
  • Packager: Tender Corporation
  • Category: HUMAN OTC DRUG LABEL

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 9, 2017

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active Ingredients - After Bite Wipe

    Ammonia 3.5%

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  • Purpose - After Bite Wipe

    Counterirritant

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  • Use - After Bite Wipe

    Temporarily protects and helps relieve minor skin irritation and itching due to - insect bites and stings, poison ivy, oak or sumac

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  • Warnings - After Bite Wipes

    For External Use Only

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  • 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

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  • Stop Use - After Bite Wipe

    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

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  • When Using - After Bite

    Do not get into eyes

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  • Directions - After Bite Wipe

    Adults and Children 2 years and older - dab directly on bite or sting, rub gently and reapply as needed

    Children under 2 years - ask a doctor

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  • Active Ingredient - Aspirin

    Aspirin (NSAID*) 325mg *nonsteroidal anti-inflammatory drug

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  • Purpose - Aspirin

    Pain Reliever/Fever Reducer

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  • When Using - Aspirin

    Reye's Syndrome: Children and teenagers who have or are recovering from chicken pox or Flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

    Allergy Alert: Aspirin may cause a severe allergic reaction which may include: hives, skin reddening, facial swelling, rash, asthma (wheezing), blisters or shock. If an allergic reaction occurs, stop use and seek medical help right away.

    Stomach bleeding warning: this contains an 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 prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen or others), have 3 or more alcoholic drinks everyday while using this problem, take more for a longer time than directed.

    Do not use if you have ever had an allergic reaction to any other pain reliever/fever reducer; right before or after heart surgery, if you are taking a prescription drug for gout, diabetes or arthritis.

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

    Ask a Doctor or Pharmacist before use if you are: under a doctor's care for any serious condition, taking any other drug.

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

    Stop use and Ask a Doctor if: you experience any of the following signs of stomach bleeding, you feel faint, vomit blood, have bloody or black stools, have stomach pain that does not get better, gets worse or lasts more than 10 days, fever gets worse or lasts more than 3 days, you have difficulty swallowing, if ringing in the ears or loss of hearing occurs, redness or swelling is present in painful areas, or any new symptoms appear.

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

    Keep out of reach of Children. In case of overdose, get medical help or contact a poison control center right away.

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  • Directions - Aspirin

    Do not use more than directed - the smallest effective dosage should be used. Drink a full glass of water with each dose. Do not take longer than 10 days, unless directed by a doctor.

    Adults and Children (12 years and older): take 1 or 2 tablets with water every 4 hours as needed. Do not take more than 12 tablets in 24 hours or as directed as a doctor.

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

    Avoid excessive heat and humidity, do not use any open or torn packets.

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  • Use - Aspirin

    Temporariy relieves minor aches and pains associated with: headache, muscular aches, minor arthritis pain, backache, common cold, toothache, menstrual cramps, temorarily reduces fever.

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  • Active Ingredient - Ibuprofen

    Ibuprofen

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  • Purpose - Ibuprofen

    Pain Reliever/Fever Reducer

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  • Use - 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.

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  • Warnings and Precautions - 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, and 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 if you have ever had an allergic reaction to any other pain reliever/fever reducer, fight before or after heart surgery.

    Ask a doctor before use if stomach bleeding warning applies to you, you have had 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 doctor 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 this product take with food or milk if stomach upset occurs.

    Stop use and ask a doctor if you experience any of the following signs of stomach bleeding, feeling faint, vomit blood, have bloody or black stools, have stomach pain that does not 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.

    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. In case of overdose, get medical help or contact a poison control center right away.

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

    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, 3 tablets may be use. Do not exceed 6 tablets in 24 hours, unless directed by a doctor. Children under 12 years: do not give children under 12 years of age.

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  • Active Ingredient - APAP

    Acetaminophen 500mg

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  • Purpose - APAP

    Analgesic/antipyretic

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  • Uses - APAP

    Temporary relief of minor aches and pains associated with: common cold, headache, toothache, muscular aches, backache, arthritis, menstrual cramps, and reduction of fever

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  • Warnings and Precautions - APAP

    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 ever day while using this product.

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

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

    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 for children even if you do not notice any signs or symptoms. Do not exceed recommended dosage.

    Store at 59-86 degrees F (15-30 degrees C), tamper evident sealed packets, do not use any open or torn packets.

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  • Directions - APAP

    Adult and Children (12 years and older) take 2 tablets every 4 to 6 hours as needed. Do not take more than 12 tablets in 24 hours.

    Children 6-11 years take 1 tablet every 4 to 6 hours as needed. Do not take more than 5 tablets in 24 hours.

    Childen under 6 do not use this product

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  • Active Ingredient - Diphenhydramine

    Diphenhydramine Hydrochloride 25mg

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  • Purpose - Diphenhydramine

    Antihistamine

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  • Use - Diphenhydramine

    Temporarily relieves these symptoms due to hay fever or other respiratory allergies: runny nose, sneezing, itching nose or throat, itchy-watery eyes.

    Temporarily relieves these symptoms due to the common cold: runny nose, sneezing

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  • Warnings and Precautions - Diphenhydramine

    Do not use to make a child sleepy or with any other product containing diphenhydramine, even one that is used on skin.

    Ask a doctor before use if you have: a breathing problem such as emphysema or chronic bronchitis, difficulty in urination due to enlargement of the prostate gland, or glaucoma.

    Ask a doctor pharmacist before you use if you are taking sedatives or tranquilizers.

    When using this product: marked drowsiness may occur, avoid alcoholic beverages, alcohol, sedatives and tranquilizers may increase the drowsiness effect, use caution when driving a motor vehicle or operating machinery, excitability may occur, especially in children.

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

    Keep out of reach of Children. In case of overdose, contact a physician or poison control center immediately.

    Each caplet may contain calcium 25mg. Store at room temperature 59-86 degrees F (15-30 C), protect from light and use by expiration date on packet. Tamper-evident sealed packets, do not use any opened or torn packets.

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  • Directions - Diphenhydramine

    Do not use more than directed.

    Adults and Children (12 Years and older) - take 1 to 2 caplets every 4 to 6 hours as needed. Do not take more than 12 caplets in 24 hours, or as directed by a doctor.

    Do not give to children under 12 years of age.

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  • Active Ingredients - After Cuts and Scrapes

    Lidocaine Hydrochloride 2.5%

    Benzalkonium Chloride .13%

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  • Purpose - After Cuts and Scrapes

    Anesthetic

    Antiseptic

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  • Uses - After Cuts and Scrapes

    First aid for the temporary relief of pain and to protect from infection in minor cuts, scrapes and burns.

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  • Warnings and Precautions - After Cuts and Scrapes

    For External Use Only.

    When using this product: do not get into eyes, do not use in large quantities, particularly over raw surfaces or blistered areas.

    Stop use and ask a doctor if rash, redness or swelling occurs or pain increases. In case of deep puncture wounds, animal bites or serious burns consult a doctor.

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

    If in eyes, flush with water for 15 minutes and call a doctor.

    Keep out of Reach of Children.

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  • Directions - After Cuts and Scrapes

    Shake Well. Clean affected area. Spray on the area 1 to 3 times daily. Adults and children 2 years and older, apply to affected area. Children under 2 years, ask a doctor.

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  • Active Ingredient - After Burn

    Lidocaine Hydrochloride 2.5%

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  • Purpose - After Burn

    Topical Analgesic

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  • Use - After Burn

    For the temporary relief of pain due to minor burns, sunburn, minor cuts, scrapes or minor skin irritations

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  • Warnings and Precautions - After Burn

    For external use only.

    When using this product: avoid contact with eyes, do not use in large quantities, particularly over raw surfaces or blistered areas, do not use longer than 1 week unless directed by a doctor, or in case of deep puncture wounds, animal bites or serious burns, consult a doctor.

    Stop use and ask a doctor if conditions or symptoms persist for more than 7 days or clear up and occur again within a few days.

    Keep out of Reach of Children.

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

    If in eyes, flush with water for 15 minutes and call a doctor

    Adults and Children 2 years and older, apply small amount to affected area, not more than 3 times daily.

    Children under 2 years, consult a doctor.

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  • Inactive Ingredients - After Burn

    Aloe Vera Gel, Benzalkonium Chloride, Carbomer 980, glycerol, USP, herbal fragrance, menthol, polysorbate 20, Propylene glycol, purified water, sodium hydroxide (50%)

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  • Package Labels
  • INGREDIENTS AND APPEARANCE
    EASY CARE FIRST AID KIT - COMPREHENSIVE 
    ammonia, aspirin, diphenhydramine hydrochloride, ibuprofen, acetaminophen, lidocaine hydrochloride, benzalkonium chloride kit
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:44224-2999
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:44224-2999-0 1 in 1 BOX; Type 0: Not a Combination Product 01/01/2012
    Quantity of Parts
    Part # Package Quantity Total Product Quantity
    Part 1 0 TUBE 1 mL  in 59 
    Part 2 1 PACKET
    Part 3 1 PACKET
    Part 4 2 PACKET
    Part 5 0 BOTTLE 1 mL  in 30 
    Part 6 1 PACKET
    Part 7 4 PACKAGE 3 mL  in .7 
    Part 1 of 7
    AFTER BURN 
    lidocaine hydrochloride gel
    Product Information
    Item Code (Source) NDC:44224-5120
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 25 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MENTHOL (UNII: L7T10EIP3A)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:44224-5120-0 59 mL 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 not final part348 04/12/2012
    Part 2 of 7
    MEDIQUE IPRIN 
    ibuprofen tablet, coated
    Product Information
    Item Code (Source) NDC:47682-700
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IBUPROFEN (UNII: WK2XYI10QM) (IBUPROFEN - UNII:WK2XYI10QM) IBUPROFEN 200 mg
    Inactive Ingredients
    Ingredient Name Strength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    TALC (UNII: 7SEV7J4R1U)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Color red (Reddish Brown) Score no score
    Shape ROUND Size 10mm
    Flavor Imprint Code G;2
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-700-99 2 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    ANDA ANDA079174 01/26/2016
    Part 3 of 7
    MEDIQUE ASPIRIN 
    aspirin tablet, film coated
    Product Information
    Item Code (Source) NDC:47682-097
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E) ASPIRIN 325 mg
    Inactive Ingredients
    Ingredient Name Strength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    Product Characteristics
    Color white (White) Score no score
    Shape ROUND (Round) Size 10mm
    Flavor Imprint Code TCL;011
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-097-99 2 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part343 12/30/2008
    Part 4 of 7
    MEDIQUE DIPHEN 
    diphenhydramine hydrochloride tablet, film coated
    Product Information
    Item Code (Source) NDC:47682-184
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg
    Inactive Ingredients
    Ingredient Name Strength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    D&C RED NO. 27 (UNII: 2LRS185U6K)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    Color pink (pink) Score no score
    Shape OVAL (OVAL) Size 11mm
    Flavor Imprint Code 061;T
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-184-46 1 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 01/01/2012
    Part 5 of 7
    AFTER CUTS AND SCRAPES 
    lidocaine hydrochloride, benzalkonium chloride solution
    Product Information
    Item Code (Source) NDC:44224-3300
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 26 mg  in 1 mL
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 25 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SORBITOL (UNII: 506T60A25R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:44224-3300-0 30 mL in 1 BOTTLE; 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 07/11/2003
    Part 6 of 7
    MEDIQUE APAP EXTRA STRENGTH 
    acetaminophen tablet, film coated
    Product Information
    Item Code (Source) NDC:47682-125
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 500 mg
    Inactive Ingredients
    Ingredient Name Strength
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    POVIDONE (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    Color white Score no score
    Shape ROUND Size 12mm
    Flavor Imprint Code FR;33
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47682-125-99 2 in 1 PACKET; 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 part343 12/30/2008
    Part 7 of 7
    AFTER BITE WIPE 
    ammonia swab
    Product Information
    Item Code (Source) NDC:44224-0001
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA 30 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    DIMETHICONE 1000 (UNII: MCU2324216)  
    C12-13 ALCOHOLS (UNII: T7ZJT3I9X2)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:44224-0001-2 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 part348 01/01/2017
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 01/01/2012
    Labeler - Tender Corporation (064437304)
    Registrant - Tender Corporation (064437304)
    Establishment
    Name Address ID/FEI Business Operations
    Tender Corporation 064437304 manufacture(44224-2999)
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