Label: AMAZON BASIC CARE ACETAMINOPHEN- acetaminophen tablet

  • NDC Code(s): 72288-692-01, 72288-692-10, 72288-692-20, 72288-692-50
  • Packager: Amazon.com Services LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 17, 2024

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  • Drug Facts

    Active ingredient (in each caplet)

    Acetaminophen USP 500 mg

  • 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 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 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.

  • PREGNANCY OR BREAST FEEDING

    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.

  • Directions

    • do not take more than directed (see overdose warning)
    adults and children 12 years 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 use for more than 10 days unless directed by a doctor
    children under 12 years
    		ask a doctor

  • Other information

    • store between 20° to 25°C (68° to 77°F)
    • do not use if carton is open or if printed foil seal under cap is torn or missing.
  • Inactive ingredients

    povidone, pregelatinized starch (maize), stearic acid.

  • Questions or comments?

    call 1-855-274-4122

    DISTRIBUTED BY:
    AMAZON.COM SERVICES LLC
    410 TERRY AVENUE N.
    SEATTLE, WA 98109

    Made in India

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL 500 mg (100 Caplets Bottle)

    amazon
    basic+care

    Extra Strength
    NDC 72288-692-10

    See New Warnings Information
    & Directions

    Acetaminophen
    Caplets 500 mg
    Pain Reliever/Fever Reducer
    For Adults
    Contains No Aspirin

    100 CAPLETS
    500 mg EACH
    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL 500 mg (100 Caplets Bottle)

  • PACKAGE LABEL-PRINCIPAL DISPLAY PANEL 500 mg (100 Caplets Bottle Carton)

    amazon
    basic+care

    Extra Strength
    NDC 72288-692-10
    Compare to
    Extra Strength
    Tylenol® Caplets
    active ingredient*

    See New Warnings Information & Directions

    Acetaminophen
    Caplets 500 mg
    Pain Reliever/Fever Reducer
    For Adults
    Contains No Aspirin

    100 CAPLETS
    500 mg EACH


    PACKAGE LABEL-PRINCIPAL DISPLAY PANEL 500 mg (100 Caplets Bottle)
  • INGREDIENTS AND APPEARANCE
    AMAZON BASIC CARE ACETAMINOPHEN 
    acetaminophen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72288-692
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    POVIDONE K30 (UNII: U725QWY32X)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    PALMITOSTEARIC ACID (UNII: Q8Y7S3B85M)  
    Product Characteristics
    ColorWHITE (White to off White) Scoreno score
    ShapeCAPSULE (Biconvex) Size18mm
    FlavorImprint Code N79
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72288-692-101 in 1 CARTON05/15/2024
    1100 in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:72288-692-20200 in 1 BOTTLE; Type 0: Not a Combination Product05/15/2024
    3NDC:72288-692-50500 in 1 BOTTLE; Type 0: Not a Combination Product05/15/2024
    4NDC:72288-692-011000 in 1 BOTTLE; Type 0: Not a Combination Product05/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01305/15/2024
    Labeler - Amazon.com Services LLC (128990418)
    Registrant - Aurohealth LLC (078728447)
    Establishment
    NameAddressID/FEIBusiness Operations
    APL HEALTHCARE LIMITED650844777ANALYSIS(72288-692) , MANUFACTURE(72288-692)
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