Label: MEDIQUE APAP EXTRA STRENGTH- acetaminophen tablet, film coated
MEDI-FIRST NON-ASPIRIN EXTRA STRENGTH- acetaminophen tablet, film coated
MEDI FIRST PLUS NON-ASPIRIN EXTRA STRENGTH- acetaminophen tablet, film coated

  • NDC Code(s): 47682-175-13, 47682-175-33, 47682-175-48, 47682-175-64, view more
    47682-175-99, 47682-804-13, 47682-804-33, 47682-804-48, 47682-804-50, 47682-804-99, 47682-904-33, 47682-904-48
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 27, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient (in each tablet)

    Acetaminophen 500 mg

  • PURPOSE

    Purpose

    Pain reliever/fever reducer

  • INDICATIONS & USAGE

    Uses

    temporarily relieves minor aches and pains due to:

    • headache
    • muscular aches
    • minor pain of arthritis
    • backahe
    • the common cold
    • toothache
    • premenstrual and menstrual cramps

    temporarily reduces fever

  • WARNINGS

    Warnings

    Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:

    • more than 4,000 mg in 24 hours, which is the maximum daily amount
    • with other drugs containing acetaminophen
    • 3 or more alcoholic drinks every day while using this product

    Allergy alert:

    Acetaminophen may cause severe skin reactions. Symptoms may include:

    • skin reddening
    • blisters
    • rash

    If a skin reaction occurs, stop use and seek medical help right away.

  • DO NOT USE

    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.
    • if you are allergic to acetaminophen or any of the inactive ingredients in this product
  • ASK DOCTOR

    Ask a doctor before use if you have

    • liver disease
  • ASK DOCTOR/PHARMACIST

    Ask a doctor or pharmacist before use if

    • you are taking the blood thinning drug warfarin
  • STOP USE

    Stop use and ask a doctor if

    • 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

    These could be signs of a serious condition.

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

    Keep out of reach of children.

    Overdose warning:

    In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

  • DOSAGE & ADMINISTRATION

    Directions

    • do not use more than directed (see overdose warning)

    ​
    Adults and children: (12 years and over)

    • take 2 tablets every 6 hours while symptoms last.
    • do not take more than 6 tablets in 24 hours, unless directed by a doctor
    • do not use for more than 10 days unless directed by a doctor

    Children under 12 years: Ask a doctor

  • OTHER SAFETY INFORMATION

    Other information

    • store at room temperature 59º-86ºF (15º-30ºC)
    • tamper-evident sealed packets
    • do not use any opened or torn packets
  • INACTIVE INGREDIENT

    Inactive ingredients

    corn starch*, hypromellose*, polyethylene glycol*, povidone (K-30)*, pregelatinized starch*,purified water*, sodium starch glycolate, stearic acid*, titanium dioxide*

    *may contain

  • QUESTIONS

    Questions or comments? 1-800-634-7680

  • Medi-First Extra Strength Non Aspirin

    Medi-First®

    Extra Strength

    Non-Aspirin

    Pain Reliever/Fever Reducer

    Aches, Fever ● Acetaminophen 500mg

    Pull to Open

    Compare active ingredient to:

    Extra Strength Tylenol®

    Registered Trademark of McNeil Consumer Products

    This Package is for Households without Young Children.

    Tamper Evident Unit Dose Packets

    100 Tablets

    (50 x 2)

    175R 80433 11-6-23 AH

  • Medi First Plus Extra Strength Non-Aspirin

    Medi First®

    Plus

    Extra Strength

    Non-Aspirin

    Acetaminophen 500 mg

    Pull To Open

    This Package is For Households Without Young Children.

    Pain Reliever/Fever Reducer

    Compare Active ingredient to:

    Extra Strength Tylenol®

    Registered Trademark of McNeil Consumer

    Tamper Evident Unit Dose Packets

    100 Tablets

    (50 x 2's)

    175R 90433 11-6-23 AH

  • Medique Extra Strength APAP

    Medique®

    Extra Strength

    APAP

    Non-Aspirin Tablets

    This Package is For Households Without Young Children

    Pain Reliever/Fever Reducer ● Acetaminophen 500mg

    Compare active ingredient to Tylenol®

    Registered McNeil Consumer Products

    Tamper Evident Unit Dose Packets

    175R APAPXS 17564 11-6-23 AH

  • INGREDIENTS AND APPEARANCE
    MEDIQUE APAP EXTRA STRENGTH 
    acetaminophen tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-175
    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 (UNII: 3WJQ0SDW1A)  
    POVIDONE (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Colorwhite (white) Scoreno score
    ShapeROUND (ROUND) Size12mm
    FlavorImprint Code AZ;235
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-175-992 in 1 PACKET; Type 0: Not a Combination Product12/30/2008
    2NDC:47682-175-13250 in 1 BOX12/30/2008
    22 in 1 PACKET; Type 0: Not a Combination Product
    3NDC:47682-175-3350 in 1 BOX12/30/2008
    32 in 1 PACKET; Type 0: Not a Combination Product
    4NDC:47682-175-48125 in 1 BOX12/30/2008
    42 in 1 PACKET; Type 0: Not a Combination Product
    5NDC:47682-175-6412 in 1 BOX12/30/2008
    52 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01312/30/2008
    MEDI-FIRST NON-ASPIRIN EXTRA STRENGTH 
    acetaminophen tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-804
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
    POVIDONE (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Colorwhite (white) Scoreno score
    ShapeROUND (ROUND) Size12mm
    FlavorImprint Code AZ;235
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-804-3350 in 1 BOX12/30/2008
    12 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:47682-804-48125 in 1 BOX12/30/2008
    22 in 1 PACKET; Type 0: Not a Combination Product
    3NDC:47682-804-13250 in 1 BOX12/30/2008
    32 in 1 PACKET; Type 0: Not a Combination Product
    4NDC:47682-804-992 in 1 PACKET; Type 0: Not a Combination Product12/30/2008
    5NDC:47682-804-5025 in 1 BOX12/30/2008
    52 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01312/30/2008
    MEDI FIRST PLUS NON-ASPIRIN EXTRA STRENGTH 
    acetaminophen tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-904
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
    POVIDONE (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Colorwhite (white) Scoreno score
    ShapeROUND (ROUND) Size12mm
    FlavorImprint Code AZ;235
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-904-3350 in 1 BOX12/30/2008
    12 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:47682-904-48125 in 1 BOX12/30/2008
    22 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01312/30/2008
    Labeler - Unifirst First Aid Corporation (832947092)
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