Label: RIGHT REMEDIES PAIN RELIEF EXTRA STRENGTH CAPLET- acetaminophen tablet, coated

  • NDC Code(s): 70692-150-05, 70692-150-20, 70692-150-31, 70692-150-44
  • Packager: Strive Pharmaceuticals Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 21, 2023

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  • Drug Facts

  • Active Ingredient (in each caplet)

    Acetaminophen 500mg

  • Purpose

    Pain reliever/fever reducer

  • Uses

    • temporarily relieves minor aches and pains due to:
         • the common cold    • headache
         • backache               • minor pain of arthritis
         • toothache              • muscular aches
         • premenstrual and menstrual cramps
    • temporarily reduces fever.

  • Warnings

    Liver warning: This product contains acetaminophen.
    Severe liver damage may occur if you take:
    • more than 4,000 mg of acetaminophen in 24 hours
    • 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
    • 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 have ever had an allergic reaction to this product or any of its ingredients.

    Ask a doctor before use if you have liver disease
    Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.

    Stop use and ask a doctor if • 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.
    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. Prompt medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

  • Directions

    Do not take more than directed. See overdose warning

     adult & children
    12 years of age
    and over

     • take 2 caplets every 6 hours while symptoms last

     • do not take more than 6 caplets in 24 hours unless directed by a doctor

     • do not take more than 10 days, unless directed by a doctor
     children under

    12 years of age

    		 • ask a doctor

  • Other information

    • each caplet contains: sodium 1 mg (very low sodium)
    • store at room temperature between 20 - 25ºC (68-77ºF).
    • avoid excessive heat, cold and humidity.
    • close cap tightly after use.

  • Inactive ingredients

    croscarmellose sodium, lactose monohydrate, magnesium stearate, polyethylene glycol, polyvinyl alcohol, povidone k30, purified water, sodium starch glycolate, starch corn, talc, titanium dioxide

  • Questions or comments?

    1-888-577-8033  Monday - Friday 8am - 4pm EST

  • SPL UNCLASSIFIED SECTION

    *compare to the active ingredient of Extra Strength Tylenol®

    TAMPER EVIDENT. DO NOT USE IF IMPRINTED SEAL UNDER CAP IS BROKEN OR MISSING FROM BOTTLE

    Distributed by: Strive Pharmaceuticals inc. East Brunswick, NJ 08816

    Product of India

    Packaged & Quality Assured in USA

    READ AND KEEP OUTER PACKAGE FOR COMPLETE PRODUCT INFORMATION

    *This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division., owner of the registered trademark Tylenol® Extra Strength Caplets.

    REV.00- 102022

  • Packaging

    Strive-150strive-150

  • INGREDIENTS AND APPEARANCE
    RIGHT REMEDIES PAIN RELIEF EXTRA STRENGTH CAPLET 
    acetaminophen tablet, coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70692-150
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    POVIDONE K30 (UNII: U725QWY32X)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapecapsuleSize18mm
    FlavorImprint Code S150
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70692-150-0550 in 1 PACKAGE; Type 0: Not a Combination Product07/20/2022
    2NDC:70692-150-20200 in 1 BOTTLE; Type 0: Not a Combination Product07/20/2022
    3NDC:70692-150-441 in 1 CARTON11/21/2023
    340 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    4NDC:70692-150-31300 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/21/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01307/20/2022
    Labeler - Strive Pharmaceuticals Inc. (080028013)
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